ENST00000381418.9:c.3450T>A
MANE Select
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ENSP00000370826.4:p.Ala1150=
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ENST00000680789.1:c.3450T>A
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ENSP00000505181.1:p.Ala1150=
|
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ENST00000312841.9:c.3285T>A
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ENSP00000326765.8:p.Ala1095=
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ENST00000381418.8:c.3450T>A
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ENSP00000370826.4:p.Ala1150=
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ENST00000522016.1:n.1643T>A
|
|
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NM_005144.4:c.3450T>A
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NP_005135.2:p.Ala1150=
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NM_018411.4:c.3285T>A
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NP_060881.2:p.Ala1095=
|
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XM_005273569.1:c.3453T>A
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XP_005273626.1:p.Ala1151=
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XM_006716367.1:c.3288T>A
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XP_006716430.1:p.Ala1096=
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XM_005273569.2:c.3453T>A
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XP_005273626.1:p.Ala1151=
|
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XM_006716367.2:c.3288T>A
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XP_006716430.1:p.Ala1096=
|
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NM_005144.5:c.3450T>A
MANE Select
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NP_005135.2:p.Ala1150=
|
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