ENST00000698724.1:n.1941+39T>A
|
|
|
ENST00000698725.1:n.1694+39T>A
|
|
|
ENST00000698726.1:n.3254+39T>A
|
|
|
ENST00000698727.1:n.2987+39T>A
|
|
|
ENST00000698728.1:n.3603+39T>A
|
|
|
ENST00000698729.1:n.5051+39T>A
|
|
|
ENST00000698730.1:n.5149+39T>A
|
|
|
ENST00000698731.1:c.3883+39T>A
|
ENSP00000513898.1:n.3883+39T>A
|
|
ENST00000698732.1:c.*2713+39T>A
|
ENSP00000513899.1:n.*2713+39T>A
|
|
ENST00000698733.1:c.*3211+39T>A
|
ENSP00000513900.1:n.*3211+39T>A
|
|
ENST00000698734.1:c.*2197+39T>A
|
ENSP00000513901.1:n.*2197+39T>A
|
|
ENST00000698735.1:n.4375+39T>A
|
|
|
ENST00000698736.1:n.4788+39T>A
|
|
|
ENST00000698737.1:n.4178T>A
|
|
|
ENST00000372371.8:c.4024+39T>A
MANE Select
|
ENSP00000361446.3:n.4024+39T>A
|
|
ENST00000372371.7:c.4024+39T>A
|
ENSP00000361446.3:n.4024+39T>A
|
|
ENST00000616246.4:c.472+39T>A
|
ENSP00000483738.1:n.472+39T>A
|
|
NM_007055.3:c.4024+39T>A
|
NP_008986.2:n.4024+39T>A
|
|
NM_007055.4:c.4024+39T>A
MANE Select
|
NP_008986.2:n.4024+39T>A
|
|