ENST00000470094.2:c.8703T>A
|
ENSP00000434898.2:p.Gly2901=
|
|
ENST00000528762.2:c.*70T>A
|
ENSP00000433168.2:n.*70T>A
|
|
ENST00000530893.7:c.8334T>A
|
ENSP00000499438.2:p.Gly2778=
|
|
ENST00000665585.2:c.*265T>A
|
ENSP00000499570.2:n.*265T>A
|
|
ENST00000666593.2:c.8703T>A
|
ENSP00000499256.2:p.Gly2901=
|
|
ENST00000700202.2:c.8703T>A
|
ENSP00000514856.2:p.Gly2901=
|
|
ENST00000700202.1:c.1170T>A
|
ENSP00000514856.1:p.Gly390=
|
|
ENST00000700203.1:n.830T>A
|
|
|
ENST00000380152.8:c.8703T>A
MANE Select
|
ENSP00000369497.3:p.Gly2901=
|
|
ENST00000544455.6:c.8703T>A
|
ENSP00000439902.1:p.Gly2901=
|
|
ENST00000614259.2:c.8711T>A
|
ENSP00000506251.1:n.8711T>A
|
|
ENST00000665585.1:c.1581T>A
|
|
|
ENST00000680887.1:c.8703T>A
|
ENSP00000505508.1:p.Gly2901=
|
|
ENST00000380152.7:c.8703T>A
|
ENSP00000369497.3:p.Gly2901=
|
|
ENST00000528762.1:c.265T>A
|
ENSP00000433168.1:n.265T>A
|
|
ENST00000544455.5:c.8703T>A
|
ENSP00000439902.1:p.Gly2901=
|
|
NM_000059.3:c.8703T>A , LRG_293t1:c.8703T>A
|
NP_000050.2:p.Gly2901=
|
|
XM_011535203.1:c.8703T>A
|
XP_011533505.1:p.Gly2901=
|
|
XM_011535204.1:c.8607T>A
|
XP_011533506.1:p.Gly2869=
|
|
XM_011535205.1:c.8703T>A
|
XP_011533507.1:p.Gly2901=
|
|
NM_000059.4:c.8703T>A
MANE Select
|
NP_000050.3:p.Gly2901=
|
|