ENST00000443218.2:c.-372G>T
|
ENSP00000390691.2:n.-372G>T
|
|
ENST00000446285.6:c.-128+249G>T
|
ENSP00000514632.1:n.-128+249G>T
|
|
ENST00000699835.1:c.-816G>T
|
ENSP00000514633.1:n.-816G>T
|
|
ENST00000699836.1:c.-18+249G>T
|
ENSP00000514634.1:n.-18+249G>T
|
|
ENST00000234111.9:c.-128+249G>T
MANE Select
|
ENSP00000234111.4:n.-128+249G>T
|
|
ENST00000234111.8:c.-128+249G>T
|
ENSP00000234111.4:n.-128+249G>T
|
|
ENST00000446285.5:n.189+249G>T
|
|
|
NM_001287188.1:c.-415+249G>T
|
NP_001274117.1:n.-415+249G>T
|
|
NM_002539.2:c.-128+249G>T
|
NP_002530.1:n.-128+249G>T
|
|
NM_002539.3:c.-128+249G>T
MANE Select
|
NP_002530.1:n.-128+249G>T
|
|
NM_001287188.2:c.-415+249G>T
|
NP_001274117.1:n.-415+249G>T
|
|
NM_001287189.2:c.-526G>T
|
NP_001274118.1:n.-526G>T
|
|
NM_001287190.2:c.-372G>T
|
NP_001274119.1:n.-372G>T
|
|