ENST00000261918.9:c.379G=
MANE Select
|
ENSP00000261918.4:p.Glu127=
|
|
ENST00000542748.6:c.-117G=
|
ENSP00000441493.1:n.-117G=
|
|
ENST00000261918.8:c.379G=
|
ENSP00000261918.4:p.Glu127=
|
|
ENST00000542748.5:c.-117G=
|
ENSP00000441493.1:n.-117G=
|
|
ENST00000543145.6:c.337G=
|
ENSP00000438966.2:p.Glu113=
|
|
ENST00000567345.1:c.-117G=
|
ENSP00000454365.1:n.-117G=
|
|
NM_001146029.1:c.337G=
|
NP_001139501.1:p.Glu113=
|
|
NM_001146030.1:c.-117G=
|
NP_001139502.1:n.-117G=
|
|
NM_003612.3:c.379G=
|
NP_003603.1:p.Glu127=
|
|
NM_001146029.2:c.337G=
|
NP_001139501.1:p.Glu113=
|
|
NM_001146030.2:c.-117G=
|
NP_001139502.1:n.-117G=
|
|
NM_003612.4:c.379G=
|
NP_003603.1:p.Glu127=
|
|
NM_003612.5:c.379G=
MANE Select
|
NP_003603.1:p.Glu127=
|
|
NM_001146029.3:c.337G=
|
NP_001139501.1:p.Glu113=
|
|
NM_001146030.3:c.-117G=
|
NP_001139502.1:n.-117G=
|
|