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NM_006767.4:c.1942G>T
MANE Select
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NP_006758.2:p.Gly648Cys
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ENST00000646124.2:c.1942G>T
MANE Select
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ENSP00000496779.1:p.Gly648Cys
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NM_006767.3:c.1942G>T
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NP_006758.2:p.Gly648Cys
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ENST00000215739.12:c.1942G>T
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ENSP00000215739.8:p.Gly648Cys
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ENST00000415354.6:c.254G>T
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ENSP00000393765.2:p.Trp85Leu
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ENST00000415817.2:c.254G>T
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ENST00000439171.5:c.224G>T
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ENST00000452988.5:c.121G>T
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ENSP00000408789.1:p.Gly41Ter
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ENST00000464807.1:n.203G>T
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ENST00000479606.5:n.2088G>T
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ENST00000491432.5:n.363G>T
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ENST00000495142.5:n.558G>T
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ENST00000495142.6:n.1575G>T
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ENST00000642151.1:c.1773G>T
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ENST00000643578.1:n.1964G>T
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ENST00000643710.1:n.803G>T
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ENST00000646506.1:n.1809G>T
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ENST00000700578.1:c.1942G>T
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ENSP00000515073.1:p.Gly648Cys
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