ENST00000369538.4:c.22+2162G>T
|
ENSP00000358551.4:n.22+2162G>T
|
|
ENST00000520113.7:c.34+148G>T
MANE Select
|
ENSP00000430075.3:n.34+148G>T
|
|
ENST00000637080.1:c.37+2149G>T
|
ENSP00000489753.1:n.37+2149G>T
|
|
ENST00000369538.3:c.121+2162G>T
|
ENSP00000358551.3:n.121+2162G>T
|
|
ENST00000520113.6:c.133+148G>T
|
ENSP00000430075.2:n.133+148G>T
|
|
NM_000036.2:c.133+148G>T
|
NP_000027.2:n.133+148G>T
|
|
NM_001172626.1:c.121+2162G>T
|
NP_001166097.1:n.121+2162G>T
|
|
NM_000036.3:c.34+148G>T
MANE Select
|
NP_000027.3:n.34+148G>T
|
|
NM_001172626.2:c.22+2162G>T
|
NP_001166097.2:n.22+2162G>T
|
|