ENST00000585465.3:c.*2745C>A
|
ENSP00000490268.2:n.*2745C>A
|
|
ENST00000585748.3:c.772C>A
|
ENSP00000477641.2:p.Gln258Lys
|
|
ENST00000585851.2:c.970C>A
|
ENSP00000467912.2:p.Gln324Lys
|
|
ENST00000326873.12:c.1144C>A
MANE Select
|
ENSP00000324856.6:p.Gln382Lys
|
|
ENST00000326873.11:c.1144C>A
|
ENSP00000324856.6:p.Gln382Lys
|
|
ENST00000585465.2:n.2877C>A
|
|
|
ENST00000586243.5:c.1144C>A
|
ENSP00000467240.2:p.Gln382Lys
|
|
ENST00000589152.5:n.1842C>A
|
|
|
NM_000455.4:c.1144C>A , LRG_319t1:c.1144C>A
|
NP_000446.1:p.Gln382Lys
|
|
XM_005259617.1:c.1139C>A
|
XP_005259674.1:p.Thr380Lys
|
|
XM_011528209.1:c.917C>A
|
XP_011526511.1:p.Thr306Lys
|
|
XM_005259617.3:c.1139C>A
|
XP_005259674.1:p.Thr380Lys
|
|
XM_011528209.2:c.917C>A
|
XP_011526511.1:p.Thr306Lys
|
|
XR_001753738.2:n.1950C>A
|
|
|
XR_001753740.2:n.1920C>A
|
|
|
NM_000455.5:c.1144C>A
MANE Select
|
NP_000446.1:p.Gln382Lys
|
|