ENST00000269980.7:c.802G>T
MANE Select
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ENSP00000269980.2:p.Gly268Cys
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ENST00000269980.6:c.802G>T
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ENSP00000269980.2:p.Gly268Cys
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ENST00000457836.6:c.736G>T
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ENSP00000416000.2:p.Gly246Cys
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ENST00000535632.5:n.431G>T
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ENST00000540732.3:c.904G>T
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ENSP00000443246.1:p.Gly302Cys
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ENST00000542943.5:c.715G>T
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ENSP00000440345.1:p.Gly239Cys
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ENST00000545787.1:n.430G>T
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ENST00000595085.5:c.802G>T
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ENSP00000471150.2:p.Gly268Cys
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NM_000709.3:c.802G>T
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NP_000700.1:p.Gly268Cys
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NM_001164783.1:c.802G>T
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NP_001158255.1:p.Gly268Cys
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NM_000709.4:c.802G>T
MANE Select
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NP_000700.1:p.Gly268Cys
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NM_001164783.2:c.802G>T
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NP_001158255.1:p.Gly268Cys
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