ENST00000585465.3:c.*2418T>G
|
ENSP00000490268.2:n.*2418T>G
|
|
ENST00000585748.3:c.737-292T>G
|
ENSP00000477641.2:n.737-292T>G
|
|
ENST00000585851.2:c.935-292T>G
|
ENSP00000467912.2:n.935-292T>G
|
|
ENST00000326873.12:c.1109-292T>G
MANE Select
|
ENSP00000324856.6:n.1109-292T>G
|
|
ENST00000326873.11:c.1109-292T>G
|
ENSP00000324856.6:n.1109-292T>G
|
|
ENST00000585465.2:n.2550T>G
|
|
|
ENST00000586243.5:c.1109-292T>G
|
ENSP00000467240.2:n.1109-292T>G
|
|
ENST00000589152.5:n.1807-292T>G
|
|
|
NM_000455.4:c.1109-292T>G , LRG_319t1:c.1109-292T>G
|
NP_000446.1:n.1109-292T>G
|
|
XM_005259617.1:c.1109-297T>G
|
XP_005259674.1:n.1109-297T>G
|
|
XM_011528209.1:c.887-297T>G
|
XP_011526511.1:n.887-297T>G
|
|
XM_005259617.3:c.1109-297T>G
|
XP_005259674.1:n.1109-297T>G
|
|
XM_011528209.2:c.887-297T>G
|
XP_011526511.1:n.887-297T>G
|
|
XR_001753738.2:n.1915-292T>G
|
|
|
XR_001753740.2:n.1885-292T>G
|
|
|
NM_000455.5:c.1109-292T>G
MANE Select
|
NP_000446.1:n.1109-292T>G
|
|