ENST00000236671.7:c.972+12G>T
MANE Select
|
ENSP00000236671.2:n.972+12G>T
|
|
ENST00000367196.4:c.867+12G>T
|
ENSP00000356164.4:n.867+12G>T
|
|
ENST00000427721.3:c.397+12G>T
|
|
|
ENST00000429746.2:c.867+12G>T
|
ENSP00000402586.2:n.867+12G>T
|
|
ENST00000433655.6:c.*138+12G>T
|
ENSP00000404902.1:n.*138+12G>T
|
|
ENST00000438213.6:c.1089+12G>T
|
ENSP00000415036.2:n.1089+12G>T
|
|
ENST00000497544.3:n.600G>T
|
|
|
ENST00000636397.1:c.972+12G>T
|
ENSP00000489910.1:n.972+12G>T
|
|
ENST00000636571.1:c.951+12G>T
|
ENSP00000490770.1:n.951+12G>T
|
|
ENST00000636615.1:c.972+12G>T
|
ENSP00000490014.1:n.972+12G>T
|
|
ENST00000636843.1:c.966+12G>T
|
ENSP00000490897.1:n.966+12G>T
|
|
ENST00000637158.1:n.570+12G>T
|
|
|
ENST00000637381.2:n.3400+12G>T
|
|
|
ENST00000637387.1:c.972+12G>T
|
ENSP00000490598.1:n.972+12G>T
|
|
ENST00000637815.2:c.954+12G>T
|
ENSP00000490344.1:n.954+12G>T
|
|
ENST00000637915.1:c.972+12G>T
|
ENSP00000490471.1:n.972+12G>T
|
|
ENST00000637937.1:n.280+12G>T
|
|
|
ENST00000678991.1:c.*833+12G>T
|
ENSP00000503019.1:n.*833+12G>T
|
|
ENST00000236671.6:c.972+12G>T
|
ENSP00000236671.2:n.972+12G>T
|
|
ENST00000427721.2:c.372+12G>T
|
ENSP00000415840.2:n.372+12G>T
|
|
ENST00000429746.1:c.303+12G>T
|
ENSP00000402586.1:n.303+12G>T
|
|
ENST00000433655.5:c.*138+12G>T
|
ENSP00000404902.1:n.*138+12G>T
|
|
ENST00000497544.1:n.600G>T
|
|
|
NM_001909.4:c.972+12G>T
|
NP_001900.1:n.972+12G>T
|
|
NM_001909.5:c.972+12G>T
MANE Select
|
NP_001900.1:n.972+12G>T
|
|