ENST00000321612.8:c.2057A>T
MANE Select
|
ENSP00000370737.4:p.Asp686Val
|
|
ENST00000638233.1:n.492A>T
|
|
|
ENST00000638661.1:c.257A>T
|
ENSP00000491369.1:p.Asp86Val
|
|
ENST00000638694.1:n.244A>T
|
|
|
ENST00000639318.1:c.257A>T
|
ENSP00000491932.1:p.Asp86Val
|
|
ENST00000639364.1:n.1757A>T
|
|
|
ENST00000639443.1:n.1625A>T
|
|
|
ENST00000639954.1:n.1765A>T
|
|
|
ENST00000640505.1:n.296A>T
|
|
|
ENST00000321612.6:c.2057A>T
|
ENSP00000370737.3:p.Asp686Val
|
|
NM_000170.2:c.2057A>T , LRG_643t1:c.2057A>T
|
NP_000161.2:p.Asp686Val
|
|
NM_000170.3:c.2057A>T
MANE Select
|
NP_000161.2:p.Asp686Val
|
|