ENST00000251810.8:c.1034T>G
MANE Select
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ENSP00000251810.3:p.Phe345Cys
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ENST00000251810.7:c.1034T>G
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ENSP00000251810.3:p.Phe345Cys
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ENST00000395910.6:n.421T>G
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|
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ENST00000395912.6:c.878T>G
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ENSP00000379248.2:p.Phe293Cys
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ENST00000519317.5:c.398T>G
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ENSP00000430641.1:p.Phe133Cys
|
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ENST00000519962.5:c.179T>G
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ENSP00000429140.1:p.Phe60Cys
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ENST00000522368.5:c.1203T>G
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ENST00000522394.1:c.367T>G
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ENSP00000429578.1:n.367T>G
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ENST00000621845.1:c.872T>G
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ENSP00000484318.1:p.Phe291Cys
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NM_001172477.1:c.1250T>G , LRG_788t1:c.1250T>G
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NP_001165948.1:p.Phe417Cys
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NM_001172478.1:c.878T>G
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NP_001165949.1:p.Phe293Cys
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NM_015713.4:c.1034T>G , LRG_788t2:c.1034T>G
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NP_056528.2:p.Phe345Cys
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NM_001172478.2:c.878T>G
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NP_001165949.1:p.Phe293Cys
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NM_015713.5:c.1034T>G
MANE Select
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NP_056528.2:p.Phe345Cys
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