ENST00000357578.8:c.569T>C
MANE Select
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ENSP00000350191.3:p.Val190Ala
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ENST00000672352.1:c.332T>C
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ENSP00000500876.1:p.Val111Ala
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ENST00000672557.1:c.487T>C
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ENST00000672652.1:c.490T>C
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ENST00000675422.1:n.1329T>C
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ENST00000348925.2:c.569T>C
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ENSP00000314649.3:p.Val190Ala
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ENST00000357578.7:c.569T>C
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ENSP00000350191.3:p.Val190Ala
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ENST00000491546.5:c.485T>C
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ENSP00000417687.1:p.Val162Ala
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NM_001080.3:c.569T>C
MANE Select
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NP_001071.1:p.Val190Ala
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NM_170740.1:c.569T>C
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NP_733936.1:p.Val190Ala
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NM_001368954.1:c.569T>C
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NP_001355883.1:p.Val190Ala
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