ENST00000251810.8:c.1001T>G
MANE Select
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ENSP00000251810.3:p.Phe334Cys
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ENST00000251810.7:c.1001T>G
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ENSP00000251810.3:p.Phe334Cys
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ENST00000395910.6:n.388T>G
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|
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ENST00000395912.6:c.845T>G
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ENSP00000379248.2:p.Phe282Cys
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ENST00000519317.5:c.365T>G
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ENSP00000430641.1:p.Phe122Cys
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ENST00000519962.5:c.146T>G
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ENSP00000429140.1:p.Phe49Cys
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ENST00000522368.5:c.1170T>G
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ENST00000522394.1:c.334T>G
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ENSP00000429578.1:n.334T>G
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ENST00000621845.1:c.839T>G
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ENSP00000484318.1:p.Phe280Cys
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NM_001172477.1:c.1217T>G , LRG_788t1:c.1217T>G
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NP_001165948.1:p.Phe406Cys
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NM_001172478.1:c.845T>G
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NP_001165949.1:p.Phe282Cys
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NM_015713.4:c.1001T>G , LRG_788t2:c.1001T>G
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NP_056528.2:p.Phe334Cys
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NM_001172478.2:c.845T>G
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NP_001165949.1:p.Phe282Cys
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NM_015713.5:c.1001T>G
MANE Select
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NP_056528.2:p.Phe334Cys
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