ENST00000470094.2:c.*599A>T
|
ENSP00000434898.2:n.*599A>T
|
|
ENST00000528762.2:c.*1443A>T
|
ENSP00000433168.2:n.*1443A>T
|
|
ENST00000530893.7:c.9707A>T
|
ENSP00000499438.2:p.Glu3236Val
|
|
ENST00000665585.2:c.*1638A>T
|
ENSP00000499570.2:n.*1638A>T
|
|
ENST00000700202.2:c.10025A>T
|
ENSP00000514856.2:p.Glu3342Val
|
|
ENST00000700202.1:c.2492A>T
|
ENSP00000514856.1:p.Glu831Val
|
|
ENST00000700203.1:n.2203A>T
|
|
|
ENST00000380152.8:c.10076A>T
MANE Select
|
ENSP00000369497.3:p.Glu3359Val
|
|
ENST00000544455.6:c.10076A>T
|
ENSP00000439902.1:p.Glu3359Val
|
|
ENST00000614259.2:c.10084A>T
|
ENSP00000506251.1:n.10084A>T
|
|
ENST00000680887.1:c.10076A>T
|
ENSP00000505508.1:p.Glu3359Val
|
|
ENST00000380152.7:c.10076A>T
|
ENSP00000369497.3:p.Glu3359Val
|
|
ENST00000544455.5:c.10076A>T
|
ENSP00000439902.1:p.Glu3359Val
|
|
NM_000059.3:c.10076A>T , LRG_293t1:c.10076A>T
|
NP_000050.2:p.Glu3359Val
|
|
XM_011535203.1:c.10076A>T
|
XP_011533505.1:p.Glu3359Val
|
|
XM_011535204.1:c.9980A>T
|
XP_011533506.1:p.Glu3327Val
|
|
NM_000059.4:c.10076A>T
MANE Select
|
NP_000050.3:p.Glu3359Val
|
|