ENST00000698724.1:n.1875T>A
|
|
|
ENST00000698725.1:n.1628T>A
|
|
|
ENST00000698726.1:n.3188T>A
|
|
|
ENST00000698727.1:n.2921T>A
|
|
|
ENST00000698728.1:n.3537T>A
|
|
|
ENST00000698729.1:n.4985T>A
|
|
|
ENST00000698730.1:n.5083T>A
|
|
|
ENST00000698731.1:c.3817T>A
|
ENSP00000513898.1:p.Ser1273Thr
|
|
ENST00000698732.1:c.*2647T>A
|
ENSP00000513899.1:n.*2647T>A
|
|
ENST00000698733.1:c.*3145T>A
|
ENSP00000513900.1:n.*3145T>A
|
|
ENST00000698734.1:c.*2131T>A
|
ENSP00000513901.1:n.*2131T>A
|
|
ENST00000698735.1:n.4309T>A
|
|
|
ENST00000698736.1:n.4722T>A
|
|
|
ENST00000698737.1:n.4073T>A
|
|
|
ENST00000372371.8:c.3958T>A
MANE Select
|
ENSP00000361446.3:p.Ser1320Thr
|
|
ENST00000372371.7:c.3958T>A
|
ENSP00000361446.3:p.Ser1320Thr
|
|
ENST00000616246.4:c.406T>A
|
ENSP00000483738.1:p.Ser136Thr
|
|
NM_007055.3:c.3958T>A
|
NP_008986.2:p.Ser1320Thr
|
|
NM_007055.4:c.3958T>A
MANE Select
|
NP_008986.2:p.Ser1320Thr
|
|