ENST00000366930.9:c.1034T>G
MANE Select
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ENSP00000355897.4:p.Phe345Cys
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ENST00000366929.4:c.1118T>G
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ENSP00000355896.4:p.Phe373Cys
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ENST00000366930.8:c.1034T>G
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ENSP00000355897.4:p.Phe345Cys
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ENST00000479322.1:n.518T>G
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|
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NM_001135599.2:c.1118T>G
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NP_001129071.1:p.Phe373Cys
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NM_003238.3:c.1034T>G
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NP_003229.1:p.Phe345Cys
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NM_001135599.3:c.1118T>G
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NP_001129071.1:p.Phe373Cys
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NM_003238.4:c.1034T>G
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NP_003229.1:p.Phe345Cys
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NR_138148.1:n.2337T>G
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NR_138149.1:n.2421T>G
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NM_003238.5:c.1034T>G
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NP_003229.1:p.Phe345Cys
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NM_003238.6:c.1034T>G
MANE Select
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NP_003229.1:p.Phe345Cys
|
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NM_001135599.4:c.1118T>G
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NP_001129071.1:p.Phe373Cys
|
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NR_138148.2:n.2285T>G
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|
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NR_138149.2:n.2369T>G
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