ENST00000321612.8:c.2136C>T
MANE Select
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ENSP00000370737.4:p.Asp712=
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ENST00000638233.1:n.571C>T
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ENST00000638661.1:c.336C>T
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ENSP00000491369.1:p.Asp112=
|
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ENST00000638694.1:n.323C>T
|
|
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ENST00000639318.1:c.336C>T
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ENSP00000491932.1:p.Asp112=
|
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ENST00000639364.1:n.1836C>T
|
|
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ENST00000639443.1:n.1704C>T
|
|
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ENST00000639954.1:n.1844C>T
|
|
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ENST00000640505.1:n.375C>T
|
|
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ENST00000321612.6:c.2136C>T
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ENSP00000370737.3:p.Asp712=
|
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NM_000170.2:c.2136C>T , LRG_643t1:c.2136C>T
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NP_000161.2:p.Asp712=
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|
NM_000170.3:c.2136C>T
MANE Select
|
NP_000161.2:p.Asp712=
|
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