|
NM_001619.5:c.555+1G>A
MANE Select
|
NP_001610.2:n.555+1G>A
|
|
ENST00000308595.10:c.555+1G>A
MANE Select
|
ENSP00000312262.5:n.555+1G>A
|
|
NM_001619.3:c.555+1G>A
|
NP_001610.2:n.555+1G>A
|
|
NM_001619.4:c.555+1G>A
|
NP_001610.2:n.555+1G>A
|
|
ENST00000308595.9:c.555+1G>A
|
ENSP00000312262.5:n.555+1G>A
|
|
ENST00000416281.6:n.1178G>A
|
|
|
ENST00000526285.1:c.555+1G>A
|
ENSP00000434126.1:n.555+1G>A
|
|
ENST00000529738.1:n.183+884G>A
|
|
|
ENST00000533077.5:n.591G>A
|
|
|
XM_011544773.1:c.465+1G>A
|
XP_011543075.1:n.465+1G>A
|
|
XM_024448376.1:c.480+1G>A
|
XP_024304144.1:n.480+1G>A
|
|
XR_001747779.1:n.835+1G>A
|
|
|
XR_949796.1:n.855+1G>A
|
|