ENST00000698724.1:n.1941+140G>T
|
|
|
ENST00000698725.1:n.1694+140G>T
|
|
|
ENST00000698726.1:n.3254+140G>T
|
|
|
ENST00000698727.1:n.2987+140G>T
|
|
|
ENST00000698728.1:n.3603+140G>T
|
|
|
ENST00000698729.1:n.5051+140G>T
|
|
|
ENST00000698730.1:n.5149+140G>T
|
|
|
ENST00000698731.1:c.3883+140G>T
|
ENSP00000513898.1:n.3883+140G>T
|
|
ENST00000698732.1:c.*2713+140G>T
|
ENSP00000513899.1:n.*2713+140G>T
|
|
ENST00000698733.1:c.*3211+140G>T
|
ENSP00000513900.1:n.*3211+140G>T
|
|
ENST00000698734.1:c.*2197+140G>T
|
ENSP00000513901.1:n.*2197+140G>T
|
|
ENST00000698735.1:n.4375+140G>T
|
|
|
ENST00000698736.1:n.4788+140G>T
|
|
|
ENST00000372371.8:c.4024+140G>T
MANE Select
|
ENSP00000361446.3:n.4024+140G>T
|
|
ENST00000372371.7:c.4024+140G>T
|
ENSP00000361446.3:n.4024+140G>T
|
|
ENST00000616246.4:c.472+140G>T
|
ENSP00000483738.1:n.472+140G>T
|
|
NM_007055.3:c.4024+140G>T
|
NP_008986.2:n.4024+140G>T
|
|
NM_007055.4:c.4024+140G>T
MANE Select
|
NP_008986.2:n.4024+140G>T
|
|