ENST00000321612.8:c.1916G>T
MANE Select
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ENSP00000370737.4:p.Gly639Val
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ENST00000460457.2:n.76G>T
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ENST00000638233.1:n.351G>T
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ENST00000638661.1:c.116G>T
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ENSP00000491369.1:p.Gly39Val
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ENST00000638694.1:n.103G>T
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ENST00000639318.1:c.116G>T
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ENSP00000491932.1:p.Gly39Val
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ENST00000639364.1:n.1616G>T
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ENST00000639443.1:n.1484G>T
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ENST00000639954.1:n.1624G>T
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ENST00000640208.1:c.116G>T
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ENSP00000491895.1:p.Gly39Val
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ENST00000640505.1:n.155G>T
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ENST00000640592.1:n.1799G>T
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ENST00000321612.6:c.1916G>T
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ENSP00000370737.3:p.Gly639Val
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ENST00000460457.1:n.55G>T
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NM_000170.2:c.1916G>T , LRG_643t1:c.1916G>T
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NP_000161.2:p.Gly639Val
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NM_000170.3:c.1916G>T
MANE Select
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NP_000161.2:p.Gly639Val
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