ENST00000321612.8:c.2166A>T
MANE Select
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ENSP00000370737.4:p.Gly722=
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ENST00000638233.1:n.601A>T
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ENST00000638661.1:c.366A>T
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ENSP00000491369.1:p.Gly122=
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ENST00000638694.1:n.353A>T
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ENST00000639318.1:c.366A>T
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ENSP00000491932.1:p.Gly122=
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ENST00000639364.1:n.1866A>T
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ENST00000639443.1:n.1734A>T
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ENST00000639954.1:n.1874A>T
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ENST00000640505.1:n.405A>T
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ENST00000321612.6:c.2166A>T
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ENSP00000370737.3:p.Gly722=
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NM_000170.2:c.2166A>T , LRG_643t1:c.2166A>T
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NP_000161.2:p.Gly722=
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NM_000170.3:c.2166A>T
MANE Select
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NP_000161.2:p.Gly722=
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