ENST00000321612.8:c.2093C=
MANE Select
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ENSP00000370737.4:p.Thr698=
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ENST00000638233.1:n.528C=
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ENST00000638661.1:c.293C=
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ENSP00000491369.1:p.Thr98=
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ENST00000638694.1:n.280C=
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|
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ENST00000639318.1:c.293C=
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ENSP00000491932.1:p.Thr98=
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ENST00000639364.1:n.1793C=
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|
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ENST00000639443.1:n.1661C=
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|
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ENST00000639954.1:n.1801C=
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|
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ENST00000640505.1:n.332C=
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ENST00000321612.6:c.2093C=
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ENSP00000370737.3:p.Thr698=
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NM_000170.2:c.2093C= , LRG_643t1:c.2093C=
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NP_000161.2:p.Thr698=
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NM_000170.3:c.2093C=
MANE Select
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NP_000161.2:p.Thr698=
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