ENST00000321612.8:c.1955G>T
MANE Select
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ENSP00000370737.4:p.Gly652Val
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ENST00000460457.2:n.115G>T
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ENST00000638233.1:n.390G>T
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ENST00000638661.1:c.155G>T
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ENSP00000491369.1:p.Gly52Val
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ENST00000638694.1:n.142G>T
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ENST00000639318.1:c.155G>T
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ENSP00000491932.1:p.Gly52Val
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ENST00000639364.1:n.1655G>T
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ENST00000639443.1:n.1523G>T
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ENST00000639954.1:n.1663G>T
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ENST00000640208.1:c.155G>T
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ENSP00000491895.1:p.Gly52Val
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ENST00000640505.1:n.194G>T
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ENST00000640592.1:n.1838G>T
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ENST00000321612.6:c.1955G>T
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ENSP00000370737.3:p.Gly652Val
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ENST00000460457.1:n.94G>T
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NM_000170.2:c.1955G>T , LRG_643t1:c.1955G>T
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NP_000161.2:p.Gly652Val
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NM_000170.3:c.1955G>T
MANE Select
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NP_000161.2:p.Gly652Val
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