ENST00000336180.7:c.1284+15G>T
MANE Select
|
ENSP00000336740.2:n.1284+15G>T
|
|
ENST00000336180.6:c.1284+15G>T
|
ENSP00000336740.2:n.1284+15G>T
|
|
ENST00000418310.5:c.1374+15G>T
|
ENSP00000409717.1:n.1374+15G>T
|
|
ENST00000435201.5:c.1223+15G>T
|
ENSP00000414606.1:n.1223+15G>T
|
|
ENST00000483414.1:n.985G>T
|
|
|
ENST00000538333.3:c.1182+15G>T
|
ENSP00000444452.1:n.1182+15G>T
|
|
NM_001204426.1:c.1182+15G>T
|
NP_001191355.1:n.1182+15G>T
|
|
NM_002314.3:c.1284+15G>T
|
NP_002305.1:n.1284+15G>T
|
|
NM_002314.4:c.1284+15G>T
MANE Select
|
NP_002305.1:n.1284+15G>T
|
|
NM_001204426.2:c.1182+15G>T
|
NP_001191355.1:n.1182+15G>T
|
|