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PR:Q9NP59 | solute carrier family 40 member 1 (human) | | | | | |
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PR:000064156 | solute carrier family 40 member 1 sequence variant A77D (human) | | | | | |
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PR:000060327 | solute carrier family 40 member 1 sequence variant D157G (human) | | | | | |
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PR:000063417 | solute carrier family 40 member 1 sequence variant D181V (human) | | | | | |
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PR:000062578 | solute carrier family 40 member 1 sequence variant G80V (human) | | | | | |
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PR:000062122 | solute carrier family 40 member 1 sequence variant N144H (human) | | | | | |
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PR:Q9NP59 | solute carrier family 40 member 1 (human) | | | | | |
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PR:000064156 | solute carrier family 40 member 1 sequence variant A77D (human) | | | | | |
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PR:000060327 | solute carrier family 40 member 1 sequence variant D157G (human) | | | | | |
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PR:000063417 | solute carrier family 40 member 1 sequence variant D181V (human) | | | | | |
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PR:000062578 | solute carrier family 40 member 1 sequence variant G80V (human) | | | | | |
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PR:000062122 | solute carrier family 40 member 1 sequence variant N144H (human) | | | | | |