ENST00000357578.8:c.1321G>T
MANE Select
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ENSP00000350191.3:p.Gly441Trp
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ENST00000479394.2:n.436G>T
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ENST00000672352.1:c.940G>T
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ENSP00000500876.1:p.Gly314Trp
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ENST00000672652.1:c.1284G>T
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ENST00000348925.2:c.1360G>T
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ENSP00000314649.3:p.Gly454Trp
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ENST00000357578.7:c.1321G>T
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ENSP00000350191.3:p.Gly441Trp
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ENST00000479394.1:n.436G>T
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ENST00000491546.5:c.1237G>T
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ENSP00000417687.1:p.Gly413Trp
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NM_001080.3:c.1321G>T
MANE Select
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NP_001071.1:p.Gly441Trp
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NM_170740.1:c.1360G>T
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NP_733936.1:p.Gly454Trp
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NM_001368954.1:c.1177G>T
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NP_001355883.1:p.Gly393Trp
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