ENST00000682087.2:n.359T>A
|
|
|
ENST00000682241.2:c.528T>A
|
ENSP00000507600.2:p.Thr176=
|
|
ENST00000683614.2:n.359T>A
|
|
|
ENST00000682087.1:c.359T>A
|
|
|
ENST00000682241.1:c.359T>A
|
|
|
ENST00000683614.1:c.359T>A
|
|
|
ENST00000683654.1:c.528T>A
|
ENSP00000506971.1:p.Thr176=
|
|
ENST00000684461.1:n.1198T>A
|
|
|
ENST00000261590.13:c.528T>A
MANE Select
|
ENSP00000261590.8:p.Thr176=
|
|
ENST00000261590.12:c.528T>A
|
ENSP00000261590.8:p.Thr176=
|
|
ENST00000585206.1:c.528T>A
|
ENSP00000462503.1:p.Thr176=
|
|
NM_001943.3:c.528T>A , LRG_397t1:c.528T>A
|
NP_001934.2:p.Thr176=
|
|
NM_001943.4:c.528T>A
|
NP_001934.2:p.Thr176=
|
|
XM_024451095.1:c.-7T>A
|
XP_024306863.1:n.-7T>A
|
|
NM_001943.5:c.528T>A
MANE Select
|
NP_001934.2:p.Thr176=
|
|