ENST00000321612.8:c.1914G>T
MANE Select
|
ENSP00000370737.4:p.Glu638Asp
|
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ENST00000460457.2:n.74G>T
|
|
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ENST00000638233.1:n.349G>T
|
|
|
ENST00000638661.1:c.114G>T
|
ENSP00000491369.1:p.Glu38Asp
|
|
ENST00000638694.1:n.101G>T
|
|
|
ENST00000639318.1:c.114G>T
|
ENSP00000491932.1:p.Glu38Asp
|
|
ENST00000639364.1:n.1614G>T
|
|
|
ENST00000639443.1:n.1482G>T
|
|
|
ENST00000639954.1:n.1622G>T
|
|
|
ENST00000640208.1:c.114G>T
|
ENSP00000491895.1:p.Glu38Asp
|
|
ENST00000640505.1:n.153G>T
|
|
|
ENST00000640592.1:n.1797G>T
|
|
|
ENST00000321612.6:c.1914G>T
|
ENSP00000370737.3:p.Glu638Asp
|
|
ENST00000460457.1:n.53G>T
|
|
|
NM_000170.2:c.1914G>T , LRG_643t1:c.1914G>T
|
NP_000161.2:p.Glu638Asp
|
|
NM_000170.3:c.1914G>T
MANE Select
|
NP_000161.2:p.Glu638Asp
|
|