ENST00000698727.1:n.1301C>A
|
|
|
ENST00000698728.1:n.1820C>A
|
|
|
ENST00000698729.1:n.3366C>A
|
|
|
ENST00000698730.1:n.3366C>A
|
|
|
ENST00000698731.1:c.2100C>A
|
ENSP00000513898.1:p.Thr700=
|
|
ENST00000698732.1:c.*1102C>A
|
ENSP00000513899.1:n.*1102C>A
|
|
ENST00000698733.1:c.*1428C>A
|
ENSP00000513900.1:n.*1428C>A
|
|
ENST00000698734.1:c.2241C>A
|
ENSP00000513901.1:p.Thr747=
|
|
ENST00000698735.1:n.2356C>A
|
|
|
ENST00000698736.1:n.2356C>A
|
|
|
ENST00000698737.1:n.2356C>A
|
|
|
ENST00000698738.1:n.2356C>A
|
|
|
ENST00000698739.1:n.2356C>A
|
|
|
ENST00000372371.8:c.2241C>A
MANE Select
|
ENSP00000361446.3:p.Thr747=
|
|
ENST00000372371.7:c.2241C>A
|
ENSP00000361446.3:p.Thr747=
|
|
ENST00000472014.5:n.463C>A
|
|
|
ENST00000473588.2:c.904C>A
|
|
|
NM_007055.3:c.2241C>A
|
NP_008986.2:p.Thr747=
|
|
NM_007055.4:c.2241C>A
MANE Select
|
NP_008986.2:p.Thr747=
|
|