ENST00000504030.7:c.264+141G>T
MANE Select
|
ENSP00000424189.2:n.264+141G>T
|
|
ENST00000299961.5:c.219+141G>T
|
ENSP00000299961.4:n.219+141G>T
|
|
ENST00000355556.6:c.282+141G>T
|
ENSP00000347754.2:n.282+141G>T
|
|
ENST00000375498.6:c.282+141G>T
|
ENSP00000364648.2:n.282+141G>T
|
|
ENST00000504030.6:c.264+141G>T
|
ENSP00000424189.2:n.264+141G>T
|
|
ENST00000506841.6:c.264+141G>T
|
ENSP00000424776.2:n.264+141G>T
|
|
ENST00000510849.5:c.264+141G>T
|
ENSP00000423653.1:n.264+141G>T
|
|
NM_000869.5:c.282+141G>T
|
NP_000860.2:n.282+141G>T
|
|
NM_001161772.2:c.219+141G>T
|
NP_001155244.1:n.219+141G>T
|
|
NM_213621.3:c.282+141G>T
|
NP_998786.2:n.282+141G>T
|
|
NR_046363.1:n.515+141G>T
|
|
|
NM_000869.6:c.264+141G>T
MANE Select
|
NP_000860.3:n.264+141G>T
|
|
NM_213621.4:c.264+141G>T
|
NP_998786.3:n.264+141G>T
|
|
NM_001161772.3:c.219+141G>T
|
NP_001155244.1:n.219+141G>T
|
|
NR_046363.2:n.482+141G>T
|
|
|