ENST00000443218.2:c.-442G>T
|
ENSP00000390691.2:n.-442G>T
|
|
ENST00000446285.6:c.-128+179G>T
|
ENSP00000514632.1:n.-128+179G>T
|
|
ENST00000699835.1:c.-886G>T
|
ENSP00000514633.1:n.-886G>T
|
|
ENST00000699836.1:c.-18+179G>T
|
ENSP00000514634.1:n.-18+179G>T
|
|
ENST00000234111.9:c.-128+179G>T
MANE Select
|
ENSP00000234111.4:n.-128+179G>T
|
|
ENST00000234111.8:c.-128+179G>T
|
ENSP00000234111.4:n.-128+179G>T
|
|
ENST00000446285.5:n.189+179G>T
|
|
|
NM_001287188.1:c.-415+179G>T
|
NP_001274117.1:n.-415+179G>T
|
|
NM_002539.2:c.-128+179G>T
|
NP_002530.1:n.-128+179G>T
|
|
NM_002539.3:c.-128+179G>T
MANE Select
|
NP_002530.1:n.-128+179G>T
|
|
NM_001287188.2:c.-415+179G>T
|
NP_001274117.1:n.-415+179G>T
|
|
NM_001287189.2:c.-596G>T
|
NP_001274118.1:n.-596G>T
|
|
NM_001287190.2:c.-442G>T
|
NP_001274119.1:n.-442G>T
|
|