ENST00000321612.8:c.1919A>G
MANE Select
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ENSP00000370737.4:p.His640Arg
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ENST00000460457.2:n.79A>G
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ENST00000638233.1:n.354A>G
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ENST00000638661.1:c.119A>G
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ENSP00000491369.1:p.His40Arg
|
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ENST00000638694.1:n.106A>G
|
|
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ENST00000639318.1:c.119A>G
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ENSP00000491932.1:p.His40Arg
|
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ENST00000639364.1:n.1619A>G
|
|
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ENST00000639443.1:n.1487A>G
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ENST00000639954.1:n.1627A>G
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|
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ENST00000640208.1:c.119A>G
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ENSP00000491895.1:p.His40Arg
|
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ENST00000640505.1:n.158A>G
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ENST00000640592.1:n.1802A>G
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|
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ENST00000321612.6:c.1919A>G
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ENSP00000370737.3:p.His640Arg
|
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ENST00000460457.1:n.58A>G
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NM_000170.2:c.1919A>G , LRG_643t1:c.1919A>G
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NP_000161.2:p.His640Arg
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NM_000170.3:c.1919A>G
MANE Select
|
NP_000161.2:p.His640Arg
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