ENST00000470094.2:c.8812G>T
|
ENSP00000434898.2:p.Asp2938Tyr
|
|
ENST00000528762.2:c.*179G>T
|
ENSP00000433168.2:n.*179G>T
|
|
ENST00000530893.7:c.8443G>T
|
ENSP00000499438.2:p.Asp2815Tyr
|
|
ENST00000665585.2:c.*374G>T
|
ENSP00000499570.2:n.*374G>T
|
|
ENST00000666593.2:c.8812G>T
|
ENSP00000499256.2:p.Asp2938Tyr
|
|
ENST00000700202.2:c.8812G>T
|
ENSP00000514856.2:p.Asp2938Tyr
|
|
ENST00000700202.1:c.1279G>T
|
ENSP00000514856.1:p.Asp427Tyr
|
|
ENST00000700203.1:n.939G>T
|
|
|
ENST00000380152.8:c.8812G>T
MANE Select
|
ENSP00000369497.3:p.Asp2938Tyr
|
|
ENST00000544455.6:c.8812G>T
|
ENSP00000439902.1:p.Asp2938Tyr
|
|
ENST00000614259.2:c.8820G>T
|
ENSP00000506251.1:n.8820G>T
|
|
ENST00000665585.1:c.1690G>T
|
|
|
ENST00000680887.1:c.8812G>T
|
ENSP00000505508.1:p.Asp2938Tyr
|
|
ENST00000380152.7:c.8812G>T
|
ENSP00000369497.3:p.Asp2938Tyr
|
|
ENST00000528762.1:c.374G>T
|
ENSP00000433168.1:n.374G>T
|
|
ENST00000544455.5:c.8812G>T
|
ENSP00000439902.1:p.Asp2938Tyr
|
|
NM_000059.3:c.8812G>T , LRG_293t1:c.8812G>T
|
NP_000050.2:p.Asp2938Tyr
|
|
XM_011535203.1:c.8812G>T
|
XP_011533505.1:p.Asp2938Tyr
|
|
XM_011535204.1:c.8716G>T
|
XP_011533506.1:p.Asp2906Tyr
|
|
XM_011535205.1:c.8755-376G>T
|
XP_011533507.1:n.8755-376G>T
|
|
NM_000059.4:c.8812G>T
MANE Select
|
NP_000050.3:p.Asp2938Tyr
|
|