ENST00000698724.1:n.1941+4151T>A
|
|
|
ENST00000698725.1:n.3331T>A
|
|
|
ENST00000698726.1:n.4891T>A
|
|
|
ENST00000698727.1:n.4624T>A
|
|
|
ENST00000698728.1:n.5240T>A
|
|
|
ENST00000698729.1:n.6688T>A
|
|
|
ENST00000698730.1:n.6786T>A
|
|
|
ENST00000698731.1:c.*1488T>A
|
ENSP00000513898.1:n.*1488T>A
|
|
ENST00000698732.1:c.*4350T>A
|
ENSP00000513899.1:n.*4350T>A
|
|
ENST00000698733.1:c.*4848T>A
|
ENSP00000513900.1:n.*4848T>A
|
|
ENST00000698734.1:c.*3834T>A
|
ENSP00000513901.1:n.*3834T>A
|
|
ENST00000698735.1:n.6012T>A
|
|
|
ENST00000698736.1:n.6425T>A
|
|
|
ENST00000372371.8:c.*1488T>A
MANE Select
|
ENSP00000361446.3:n.*1488T>A
|
|
ENST00000372371.7:c.*1488T>A
|
ENSP00000361446.3:n.*1488T>A
|
|
ENST00000616246.4:c.472+4151T>A
|
ENSP00000483738.1:n.472+4151T>A
|
|
NM_007055.3:c.*1488T>A
|
NP_008986.2:n.*1488T>A
|
|
NM_007055.4:c.*1488T>A
MANE Select
|
NP_008986.2:n.*1488T>A
|
|