ENST00000682275.1:c.468G=
|
ENSP00000507852.1:p.Thr156=
|
|
ENST00000683395.1:c.458G=
|
|
|
ENST00000684087.1:c.468G=
|
ENSP00000506978.1:p.Thr156=
|
|
ENST00000684700.1:c.468G=
|
ENSP00000507806.1:p.Thr156=
|
|
ENST00000506362.2:c.219G=
|
ENSP00000424103.2:p.Thr73=
|
|
ENST00000673642.1:c.267G=
|
ENSP00000501242.1:p.Thr89=
|
|
ENST00000673991.1:c.468G=
|
ENSP00000501033.1:p.Thr156=
|
|
ENST00000674051.1:c.342G=
|
ENSP00000501083.1:p.Thr114=
|
|
ENST00000226760.5:c.468G=
MANE Select
|
ENSP00000226760.1:p.Thr156=
|
|
ENST00000503569.5:c.468G=
|
ENSP00000423337.1:p.Thr156=
|
|
ENST00000506362.1:c.65G=
|
|
|
ENST00000507765.1:n.653G=
|
|
|
NM_001145853.1:c.468G=
|
NP_001139325.1:p.Thr156=
|
|
NM_006005.3:c.468G=
MANE Select
|
NP_005996.2:p.Thr156=
|
|
XM_017008586.1:c.477G=
|
XP_016864075.1:p.Thr159=
|
|