ENST00000578493.2:n.1111A>T
|
|
|
ENST00000699291.1:c.903A>T
|
ENSP00000514272.1:n.903A>T
|
|
ENST00000699292.1:n.1313A>T
|
|
|
ENST00000225275.4:c.1778A>T
MANE Select
|
ENSP00000225275.3:p.Asp593Val
|
|
ENST00000225275.3:c.1778A>T
|
ENSP00000225275.3:p.Asp593Val
|
|
ENST00000577220.1:c.183+53A>T
|
ENSP00000464668.1:n.183+53A>T
|
|
NM_000250.1:c.1778A>T , LRG_84t1:c.1778A>T
|
NP_000241.1:p.Asp593Val
|
|
XM_011524821.1:c.1964A>T
|
XP_011523123.1:p.Asp655Val
|
|
XM_011524822.1:c.1493A>T
|
XP_011523124.1:p.Asp498Val
|
|
NM_000250.2:c.1778A>T
MANE Select
|
NP_000241.1:p.Asp593Val
|
|