ENST00000585465.3:c.*2738C>A
|
ENSP00000490268.2:n.*2738C>A
|
|
ENST00000585748.3:c.765C>A
|
ENSP00000477641.2:p.His255Gln
|
|
ENST00000585851.2:c.963C>A
|
ENSP00000467912.2:p.His321Gln
|
|
ENST00000326873.12:c.1137C>A
MANE Select
|
ENSP00000324856.6:p.His379Gln
|
|
ENST00000326873.11:c.1137C>A
|
ENSP00000324856.6:p.His379Gln
|
|
ENST00000585465.2:n.2870C>A
|
|
|
ENST00000586243.5:c.1137C>A
|
ENSP00000467240.2:p.His379Gln
|
|
ENST00000589152.5:n.1835C>A
|
|
|
NM_000455.4:c.1137C>A , LRG_319t1:c.1137C>A
|
NP_000446.1:p.His379Gln
|
|
XM_005259617.1:c.1132C>A
|
XP_005259674.1:p.Gln378Lys
|
|
XM_011528209.1:c.910C>A
|
XP_011526511.1:p.Gln304Lys
|
|
XM_005259617.3:c.1132C>A
|
XP_005259674.1:p.Gln378Lys
|
|
XM_011528209.2:c.910C>A
|
XP_011526511.1:p.Gln304Lys
|
|
XR_001753738.2:n.1943C>A
|
|
|
XR_001753740.2:n.1913C>A
|
|
|
NM_000455.5:c.1137C>A
MANE Select
|
NP_000446.1:p.His379Gln
|
|