ENST00000682028.1:c.36G=
|
ENSP00000507230.1:p.Glu12=
|
|
ENST00000682268.1:n.334G=
|
|
|
ENST00000682902.1:n.338G=
|
|
|
ENST00000683513.1:c.36G=
|
ENSP00000506809.1:p.Glu12=
|
|
ENST00000263431.4:c.36G=
MANE Select
|
ENSP00000263431.3:p.Glu12=
|
|
ENST00000263431.3:c.36G=
|
ENSP00000263431.3:p.Glu12=
|
|
ENST00000419486.1:c.-322-27G=
|
ENSP00000387919.2:n.-322-27G=
|
|
ENST00000474397.5:c.-322-27G=
|
ENSP00000471271.1:n.-322-27G=
|
|
ENST00000479081.5:c.-322-27G=
|
ENSP00000471544.1:n.-322-27G=
|
|
NM_001316329.1:c.36G=
|
NP_001303258.1:p.Glu12=
|
|
NM_002739.3:c.36G= , LRG_669t1:c.36G=
|
NP_002730.1:p.Glu12=
|
|
NM_002739.4:c.36G=
|
NP_002730.1:p.Glu12=
|
|
NM_002739.5:c.36G=
MANE Select
|
NP_002730.1:p.Glu12=
|
|
NM_001316329.2:c.36G=
|
NP_001303258.1:p.Glu12=
|
|