ENST00000321612.8:c.2135A>T
MANE Select
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ENSP00000370737.4:p.Asp712Val
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ENST00000638233.1:n.570A>T
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|
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ENST00000638661.1:c.335A>T
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ENSP00000491369.1:p.Asp112Val
|
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ENST00000638694.1:n.322A>T
|
|
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ENST00000639318.1:c.335A>T
|
ENSP00000491932.1:p.Asp112Val
|
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ENST00000639364.1:n.1835A>T
|
|
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ENST00000639443.1:n.1703A>T
|
|
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ENST00000639954.1:n.1843A>T
|
|
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ENST00000640505.1:n.374A>T
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|
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ENST00000321612.6:c.2135A>T
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ENSP00000370737.3:p.Asp712Val
|
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NM_000170.2:c.2135A>T , LRG_643t1:c.2135A>T
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NP_000161.2:p.Asp712Val
|
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NM_000170.3:c.2135A>T
MANE Select
|
NP_000161.2:p.Asp712Val
|
|