ENST00000251810.8:c.195A>T
MANE Select
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ENSP00000251810.3:p.Thr65=
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ENST00000251810.7:c.195A>T
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ENSP00000251810.3:p.Thr65=
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ENST00000395912.6:c.49-6124A>T
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ENSP00000379248.2:n.49-6124A>T
|
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ENST00000517517.1:n.504A>T
|
|
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ENST00000519317.5:c.48+6669A>T
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ENSP00000430641.1:n.48+6669A>T
|
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ENST00000519962.5:c.48+6669A>T
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ENSP00000429140.1:n.48+6669A>T
|
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ENST00000522368.5:c.364A>T
|
|
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ENST00000522394.1:c.122+73A>T
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ENSP00000429578.1:n.122+73A>T
|
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ENST00000523957.1:c.*118A>T
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ENSP00000427830.1:n.*118A>T
|
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ENST00000621845.1:c.33A>T
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ENSP00000484318.1:p.Thr11=
|
|
NM_001172477.1:c.411A>T , LRG_788t1:c.411A>T
|
NP_001165948.1:p.Thr137=
|
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NM_001172478.1:c.49-6124A>T
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NP_001165949.1:n.49-6124A>T
|
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NM_015713.4:c.195A>T , LRG_788t2:c.195A>T
|
NP_056528.2:p.Thr65=
|
|
NM_001172478.2:c.49-6124A>T
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NP_001165949.1:n.49-6124A>T
|
|
NM_015713.5:c.195A>T
MANE Select
|
NP_056528.2:p.Thr65=
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