ENST00000295897.9:c.1787G>T
MANE Select
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ENSP00000295897.4:p.Gly596Val
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ENST00000295897.8:c.1787G>T
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ENSP00000295897.4:p.Gly596Val
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ENST00000401494.7:c.1442G>T
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ENSP00000384695.3:p.Gly481Val
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ENST00000415165.6:c.1211G>T
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ENSP00000401820.2:p.Gly404Val
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ENST00000476441.6:c.*1066G>T
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ENSP00000423727.1:n.*1066G>T
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ENST00000495173.1:n.95G>T
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ENST00000503124.5:c.1337G>T
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ENSP00000421027.1:p.Gly446Val
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ENST00000505649.5:n.1334G>T
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ENST00000508932.5:n.177G>T
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ENST00000509063.5:c.1785+616G>T
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ENSP00000422784.1:n.1785+616G>T
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ENST00000511370.1:c.1320G>T
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ENST00000621085.4:c.1148G>T
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ENSP00000483421.1:p.Gly383Val
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ENST00000621628.4:c.1148G>T
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ENSP00000480485.1:p.Gly383Val
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NM_000477.5:c.1787G>T
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NP_000468.1:p.Gly596Val
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NM_000477.6:c.1787G>T
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NP_000468.1:p.Gly596Val
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NM_000477.7:c.1787G>T
MANE Select
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NP_000468.1:p.Gly596Val
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