ENST00000455537.7:c.2943A>T
MANE Select
|
ENSP00000408979.2:p.Thr981=
|
|
ENST00000674619.1:c.2964A>T
|
ENSP00000502270.1:p.Thr988=
|
|
ENST00000675697.1:c.34A>T
|
|
|
ENST00000675737.1:n.347A>T
|
|
|
ENST00000675882.1:n.2466A>T
|
|
|
ENST00000675929.1:n.1501A>T
|
|
|
ENST00000676055.1:c.34A>T
|
|
|
ENST00000676457.1:c.2838A>T
|
ENSP00000501588.1:p.Thr946=
|
|
ENST00000286452.5:c.2676A>T
|
ENSP00000286452.5:p.Thr892=
|
|
ENST00000455537.6:c.2943A>T
|
ENSP00000408979.2:p.Thr981=
|
|
ENST00000552227.1:n.226A>T
|
|
|
NM_004984.2:c.2943A>T
|
NP_004975.2:p.Thr981=
|
|
NM_001354705.1:c.2676A>T
|
NP_001341634.1:p.Thr892=
|
|
NM_004984.3:c.2943A>T
|
NP_004975.2:p.Thr981=
|
|
XR_002957324.1:n.3176A>T
|
|
|
NM_004984.4:c.2943A>T
MANE Select
|
NP_004975.2:p.Thr981=
|
|
NM_001354705.2:c.2676A>T
|
NP_001341634.1:p.Thr892=
|
|