ENST00000703783.1:n.201G>A
|
|
|
ENST00000703785.1:n.282G>A
|
|
|
ENST00000262464.9:c.3417G>A
MANE Select
|
ENSP00000262464.4:p.Glu1139=
|
|
ENST00000262464.8:c.3417G>A
|
ENSP00000262464.4:p.Glu1139=
|
|
ENST00000507835.5:c.-34G>A
|
ENSP00000426839.1:n.-34G>A
|
|
ENST00000508053.5:c.3417G>A
|
ENSP00000424571.1:p.Glu1139=
|
|
ENST00000508989.5:c.3318G>A
|
ENSP00000425596.1:p.Glu1106=
|
|
ENST00000619499.4:c.3414G>A
|
ENSP00000482132.1:p.Glu1138=
|
|
NM_001999.3:c.3417G>A
|
NP_001990.2:p.Glu1139=
|
|
XM_017009228.2:c.3264G>A
|
XP_016864717.1:p.Glu1088=
|
|
NM_001999.4:c.3417G>A
MANE Select
|
NP_001990.2:p.Glu1139=
|
|