ENST00000527701.6:c.*1325G=
|
ENSP00000435718.2:n.*1325G=
|
|
ENST00000533313.6:c.*1279G=
|
ENSP00000431843.2:n.*1279G=
|
|
ENST00000616349.5:c.1353G=
MANE Select
|
ENSP00000479524.2:p.Glu451=
|
|
ENST00000332271.9:c.1353G=
|
ENSP00000330031.5:p.Glu451=
|
|
ENST00000527701.5:c.1026G=
|
ENSP00000435718.1:p.Glu342=
|
|
ENST00000532537.2:n.1774G=
|
|
|
ENST00000533313.5:c.1026G=
|
ENSP00000431843.1:p.Glu342=
|
|
ENST00000616349.4:c.1353G=
|
ENSP00000479524.1:p.Glu451=
|
|
NM_001008496.3:c.1353G=
|
NP_001008496.2:p.Glu451=
|
|
NM_001255975.1:c.1353G=
MANE Select
|
NP_001242904.1:p.Glu451=
|
|
NR_045648.1:n.1984G=
|
|
|
NR_045649.1:n.1857G=
|
|
|
NR_045649.2:n.1857G=
|
|
|