ENST00000470094.2:c.9333G>A
|
ENSP00000434898.2:p.Glu3111=
|
|
ENST00000528762.2:c.*700G>A
|
ENSP00000433168.2:n.*700G>A
|
|
ENST00000530893.7:c.8964G>A
|
ENSP00000499438.2:p.Glu2988=
|
|
ENST00000665585.2:c.*895G>A
|
ENSP00000499570.2:n.*895G>A
|
|
ENST00000666593.2:c.*178G>A
|
ENSP00000499256.2:n.*178G>A
|
|
ENST00000700202.2:c.9282G>A
|
ENSP00000514856.2:p.Glu3094=
|
|
ENST00000700202.1:c.1749G>A
|
ENSP00000514856.1:p.Glu583=
|
|
ENST00000700203.1:n.1460G>A
|
|
|
ENST00000380152.8:c.9333G>A
MANE Select
|
ENSP00000369497.3:p.Glu3111=
|
|
ENST00000544455.6:c.9333G>A
|
ENSP00000439902.1:p.Glu3111=
|
|
ENST00000614259.2:c.9341G>A
|
ENSP00000506251.1:n.9341G>A
|
|
ENST00000665585.1:c.2211G>A
|
|
|
ENST00000666593.1:c.355G>A
|
ENSP00000499256.1:n.355G>A
|
|
ENST00000680887.1:c.9333G>A
|
ENSP00000505508.1:p.Glu3111=
|
|
ENST00000380152.7:c.9333G>A
|
ENSP00000369497.3:p.Glu3111=
|
|
ENST00000470094.1:c.290G>A
|
|
|
ENST00000544455.5:c.9333G>A
|
ENSP00000439902.1:p.Glu3111=
|
|
NM_000059.3:c.9333G>A , LRG_293t1:c.9333G>A
|
NP_000050.2:p.Glu3111=
|
|
XM_011535203.1:c.9333G>A
|
XP_011533505.1:p.Glu3111=
|
|
XM_011535204.1:c.9237G>A
|
XP_011533506.1:p.Glu3079=
|
|
NM_000059.4:c.9333G>A
MANE Select
|
NP_000050.3:p.Glu3111=
|
|