ENST00000585465.3:c.*2899A>T
|
ENSP00000490268.2:n.*2899A>T
|
|
ENST00000585748.3:c.926A>T
|
ENSP00000477641.2:p.Gln309Leu
|
|
ENST00000585851.2:c.1124A>T
|
ENSP00000467912.2:p.Gln375Leu
|
|
ENST00000326873.12:c.1298A>T
MANE Select
|
ENSP00000324856.6:p.Gln433Leu
|
|
ENST00000326873.11:c.1298A>T
|
ENSP00000324856.6:p.Gln433Leu
|
|
ENST00000585465.2:n.3031A>T
|
|
|
ENST00000586243.5:c.1295A>T
|
ENSP00000467240.2:p.Gln432Leu
|
|
ENST00000589152.5:n.1996A>T
|
|
|
NM_000455.4:c.1298A>T , LRG_319t1:c.1298A>T
|
NP_000446.1:p.Gln433Leu
|
|
XM_005259617.1:c.1293A>T
|
XP_005259674.1:p.Ala431=
|
|
XM_011528209.1:c.1071A>T
|
XP_011526511.1:p.Ala357=
|
|
XM_005259617.3:c.1293A>T
|
XP_005259674.1:p.Ala431=
|
|
XM_011528209.2:c.1071A>T
|
XP_011526511.1:p.Ala357=
|
|
XR_001753738.2:n.2104A>T
|
|
|
XR_001753740.2:n.2074A>T
|
|
|
NM_000455.5:c.1298A>T
MANE Select
|
NP_000446.1:p.Gln433Leu
|
|