ENST00000357578.8:c.1187T>C
MANE Select
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ENSP00000350191.3:p.Val396Ala
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ENST00000479394.2:n.302T>C
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ENST00000672352.1:c.806T>C
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ENSP00000500876.1:p.Val269Ala
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ENST00000672652.1:c.1150T>C
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ENST00000348925.2:c.1226T>C
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ENSP00000314649.3:p.Val409Ala
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ENST00000357578.7:c.1187T>C
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ENSP00000350191.3:p.Val396Ala
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ENST00000479394.1:n.302T>C
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ENST00000491546.5:c.1103T>C
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ENSP00000417687.1:p.Val368Ala
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NM_001080.3:c.1187T>C
MANE Select
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NP_001071.1:p.Val396Ala
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NM_170740.1:c.1226T>C
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NP_733936.1:p.Val409Ala
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NM_001368954.1:c.1043T>C
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NP_001355883.1:p.Val348Ala
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