ENST00000321612.8:c.1969A>T
MANE Select
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ENSP00000370737.4:p.Ser657Cys
|
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ENST00000460457.2:n.129A>T
|
|
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ENST00000638233.1:n.404A>T
|
|
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ENST00000638661.1:c.169A>T
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ENSP00000491369.1:p.Ser57Cys
|
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ENST00000638694.1:n.156A>T
|
|
|
ENST00000639318.1:c.169A>T
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ENSP00000491932.1:p.Ser57Cys
|
|
ENST00000639364.1:n.1669A>T
|
|
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ENST00000639443.1:n.1537A>T
|
|
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ENST00000639954.1:n.1677A>T
|
|
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ENST00000640208.1:c.169A>T
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ENSP00000491895.1:p.Ser57Cys
|
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ENST00000640505.1:n.208A>T
|
|
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ENST00000640592.1:n.1852A>T
|
|
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ENST00000321612.6:c.1969A>T
|
ENSP00000370737.3:p.Ser657Cys
|
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ENST00000460457.1:n.108A>T
|
|
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NM_000170.2:c.1969A>T , LRG_643t1:c.1969A>T
|
NP_000161.2:p.Ser657Cys
|
|
NM_000170.3:c.1969A>T
MANE Select
|
NP_000161.2:p.Ser657Cys
|
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