ENST00000698724.1:n.1809-39G>T
|
|
|
ENST00000698725.1:n.1523G>T
|
|
|
ENST00000698726.1:n.3122-39G>T
|
|
|
ENST00000698727.1:n.2855-39G>T
|
|
|
ENST00000698728.1:n.3471-39G>T
|
|
|
ENST00000698729.1:n.4919-39G>T
|
|
|
ENST00000698730.1:n.5017-39G>T
|
|
|
ENST00000698731.1:c.3751-39G>T
|
ENSP00000513898.1:n.3751-39G>T
|
|
ENST00000698732.1:c.*2581-39G>T
|
ENSP00000513899.1:n.*2581-39G>T
|
|
ENST00000698733.1:c.*3079-39G>T
|
ENSP00000513900.1:n.*3079-39G>T
|
|
ENST00000698734.1:c.*2065-39G>T
|
ENSP00000513901.1:n.*2065-39G>T
|
|
ENST00000698735.1:n.4243-39G>T
|
|
|
ENST00000698736.1:n.4656-39G>T
|
|
|
ENST00000698737.1:n.4007-39G>T
|
|
|
ENST00000372371.8:c.3892-39G>T
MANE Select
|
ENSP00000361446.3:n.3892-39G>T
|
|
ENST00000372371.7:c.3892-39G>T
|
ENSP00000361446.3:n.3892-39G>T
|
|
ENST00000616246.4:c.340-39G>T
|
ENSP00000483738.1:n.340-39G>T
|
|
NM_007055.3:c.3892-39G>T
|
NP_008986.2:n.3892-39G>T
|
|
NM_007055.4:c.3892-39G>T
MANE Select
|
NP_008986.2:n.3892-39G>T
|
|