ENST00000283871.10:c.1006+132C>A
MANE Select
|
ENSP00000283871.5:n.1006+132C>A
|
|
ENST00000283871.9:c.1006+132C>A
|
ENSP00000283871.5:n.1006+132C>A
|
|
ENST00000470321.1:n.346+132C>A
|
|
|
ENST00000475447.2:c.307+3266C>A
|
|
|
ENST00000492108.5:c.285+3266C>A
|
ENSP00000419838.1:n.285+3266C>A
|
|
ENST00000494453.1:c.426+132C>A
|
|
|
NM_000187.3:c.1006+132C>A
|
NP_000178.2:n.1006+132C>A
|
|
XM_005247412.1:c.781+132C>A
|
XP_005247469.1:n.781+132C>A
|
|
XM_005247413.1:c.1006+132C>A
|
XP_005247470.1:n.1006+132C>A
|
|
XM_011512746.1:c.879+3266C>A
|
XP_011511048.1:n.879+3266C>A
|
|
XM_005247412.2:c.781+132C>A
|
XP_005247469.1:n.781+132C>A
|
|
XM_005247413.2:c.1006+132C>A
|
XP_005247470.1:n.1006+132C>A
|
|
XM_011512746.2:c.879+3266C>A
|
XP_011511048.1:n.879+3266C>A
|
|
XM_017006277.2:c.583+132C>A
|
XP_016861766.1:n.583+132C>A
|
|
NM_000187.4:c.1006+132C>A
MANE Select
|
NP_000178.2:n.1006+132C>A
|
|