ENST00000321612.8:c.1922G>T
MANE Select
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ENSP00000370737.4:p.Arg641Ile
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ENST00000460457.2:n.82G>T
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|
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ENST00000638233.1:n.357G>T
|
|
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ENST00000638661.1:c.122G>T
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ENSP00000491369.1:p.Arg41Ile
|
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ENST00000638694.1:n.109G>T
|
|
|
ENST00000639318.1:c.122G>T
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ENSP00000491932.1:p.Arg41Ile
|
|
ENST00000639364.1:n.1622G>T
|
|
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ENST00000639443.1:n.1490G>T
|
|
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ENST00000639954.1:n.1630G>T
|
|
|
ENST00000640208.1:c.122G>T
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ENSP00000491895.1:p.Arg41Ile
|
|
ENST00000640505.1:n.161G>T
|
|
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ENST00000640592.1:n.1805G>T
|
|
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ENST00000321612.6:c.1922G>T
|
ENSP00000370737.3:p.Arg641Ile
|
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ENST00000460457.1:n.61G>T
|
|
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NM_000170.2:c.1922G>T , LRG_643t1:c.1922G>T
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NP_000161.2:p.Arg641Ile
|
|
NM_000170.3:c.1922G>T
MANE Select
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NP_000161.2:p.Arg641Ile
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