ENST00000376259.7:c.587T=
MANE Select
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ENSP00000365435.3:p.Met196=
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ENST00000376259.6:c.587T=
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ENSP00000365435.3:p.Met196=
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ENST00000489921.1:n.299T=
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ENST00000492361.1:n.576T=
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NM_001066.2:c.587T=
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NP_001057.1:p.Met196=
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XM_011542060.1:c.587T=
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XP_011540362.1:p.Met196=
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XM_011542061.1:c.587T=
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XP_011540363.1:p.Met196=
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XM_011542062.1:c.566T=
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XP_011540364.1:p.Met189=
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XM_011542063.1:c.587T=
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XP_011540365.1:p.Met196=
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XM_011542060.2:c.587T=
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XP_011540362.1:p.Met196=
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XM_011542063.2:c.587T=
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XP_011540365.1:p.Met196=
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XM_017002211.1:c.587T=
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XP_016857700.1:p.Met196=
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XM_017002214.1:c.2T=
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XP_016857703.1:p.Met1=
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XM_017002215.1:c.2T=
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XP_016857704.1:p.Met1=
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NM_001066.3:c.587T=
MANE Select
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NP_001057.1:p.Met196=
|
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