ENST00000348974.5:c.911A>T
|
ENSP00000330021.7:p.Glu304Val
|
|
ENST00000394236.9:c.911A>T
MANE Select
|
ENSP00000377783.3:p.Glu304Val
|
|
ENST00000407433.6:c.866A>T
|
ENSP00000385794.2:p.Glu289Val
|
|
ENST00000647936.1:c.911A>T
|
ENSP00000496822.1:p.Glu304Val
|
|
ENST00000648381.1:n.1079A>T
|
|
|
ENST00000648853.1:c.869A>T
|
ENSP00000497262.1:p.Glu290Val
|
|
ENST00000649103.1:c.1010A>T
|
ENSP00000497962.1:n.1010A>T
|
|
ENST00000650591.1:c.1007A>T
|
ENSP00000497376.1:p.Glu336Val
|
|
ENST00000394236.7:c.911A>T
|
ENSP00000377783.3:p.Glu304Val
|
|
ENST00000407433.5:c.518A>T
|
ENSP00000385794.1:p.Glu173Val
|
|
NM_000313.3:c.911A>T , LRG_572t1:c.911A>T
|
NP_000304.2:p.Glu304Val
|
|
NM_001314077.1:c.1007A>T , LRG_572t2:c.1007A>T
|
NP_001301006.1:p.Glu336Val
|
|
NM_000313.4:c.911A>T
MANE Select
|
NP_000304.2:p.Glu304Val
|
|
NM_001314077.2:c.1007A>T
|
NP_001301006.1:p.Glu336Val
|
|