ENST00000295897.9:c.1786G>T
MANE Select
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ENSP00000295897.4:p.Gly596Cys
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ENST00000295897.8:c.1786G>T
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ENSP00000295897.4:p.Gly596Cys
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ENST00000401494.7:c.1441G>T
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ENSP00000384695.3:p.Gly481Cys
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ENST00000415165.6:c.1210G>T
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ENSP00000401820.2:p.Gly404Cys
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ENST00000476441.6:c.*1065G>T
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ENSP00000423727.1:n.*1065G>T
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ENST00000495173.1:n.94G>T
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ENST00000503124.5:c.1336G>T
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ENSP00000421027.1:p.Gly446Cys
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ENST00000505649.5:n.1333G>T
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ENST00000508932.5:n.176G>T
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ENST00000509063.5:c.1785+615G>T
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ENSP00000422784.1:n.1785+615G>T
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ENST00000511370.1:c.1319G>T
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ENST00000621085.4:c.1147G>T
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ENSP00000483421.1:p.Gly383Cys
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ENST00000621628.4:c.1147G>T
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ENSP00000480485.1:p.Gly383Cys
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NM_000477.5:c.1786G>T
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NP_000468.1:p.Gly596Cys
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NM_000477.6:c.1786G>T
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NP_000468.1:p.Gly596Cys
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NM_000477.7:c.1786G>T
MANE Select
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NP_000468.1:p.Gly596Cys
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