ENST00000585465.3:c.*2807C>A
|
ENSP00000490268.2:n.*2807C>A
|
|
ENST00000585748.3:c.834C>A
|
ENSP00000477641.2:p.Thr278=
|
|
ENST00000585851.2:c.1032C>A
|
ENSP00000467912.2:p.Thr344=
|
|
ENST00000326873.12:c.1206C>A
MANE Select
|
ENSP00000324856.6:p.Thr402=
|
|
ENST00000326873.11:c.1206C>A
|
ENSP00000324856.6:p.Thr402=
|
|
ENST00000585465.2:n.2939C>A
|
|
|
ENST00000586243.5:c.1206C>A
|
ENSP00000467240.2:p.Thr402=
|
|
ENST00000589152.5:n.1904C>A
|
|
|
NM_000455.4:c.1206C>A , LRG_319t1:c.1206C>A
|
NP_000446.1:p.Thr402=
|
|
XM_005259617.1:c.1201C>A
|
XP_005259674.1:p.Gln401Lys
|
|
XM_011528209.1:c.979C>A
|
XP_011526511.1:p.Gln327Lys
|
|
XM_005259617.3:c.1201C>A
|
XP_005259674.1:p.Gln401Lys
|
|
XM_011528209.2:c.979C>A
|
XP_011526511.1:p.Gln327Lys
|
|
XR_001753738.2:n.2012C>A
|
|
|
XR_001753740.2:n.1982C>A
|
|
|
NM_000455.5:c.1206C>A
MANE Select
|
NP_000446.1:p.Thr402=
|
|