ENST00000220058.9:c.209+107G>A
MANE Select
|
ENSP00000220058.4:n.209+107G>A
|
|
ENST00000220058.8:c.209+107G>A
|
ENSP00000220058.4:n.209+107G>A
|
|
ENST00000543678.1:c.209+107G>A
|
ENSP00000443754.1:n.209+107G>A
|
|
ENST00000558460.5:c.209+107G>A
|
ENSP00000452646.1:n.209+107G>A
|
|
ENST00000558614.1:n.170+107G>A
|
|
|
ENST00000559633.1:n.128+107G>A
|
|
|
ENST00000560717.5:c.194+107G>A
|
ENSP00000457257.1:n.194+107G>A
|
|
NM_139242.3:c.209+107G>A
|
NP_640335.2:n.209+107G>A
|
|
XM_005254158.3:c.-93G>A
|
XP_005254215.1:n.-93G>A
|
|
XM_005254158.5:c.316G>A
|
XP_005254215.2:p.Ala106Thr
|
|
XR_001751081.1:n.331G>A
|
|
|
NM_139242.4:c.209+107G>A
MANE Select
|
NP_640335.2:n.209+107G>A
|
|