ENST00000269980.7:c.853+34G>A
MANE Select
|
ENSP00000269980.2:n.853+34G>A
|
|
ENST00000269980.6:c.853+34G>A
|
ENSP00000269980.2:n.853+34G>A
|
|
ENST00000457836.6:c.787+34G>A
|
ENSP00000416000.2:n.787+34G>A
|
|
ENST00000535632.5:n.482+34G>A
|
|
|
ENST00000540732.3:c.955+34G>A
|
ENSP00000443246.1:n.955+34G>A
|
|
ENST00000542943.5:c.766+34G>A
|
ENSP00000440345.1:n.766+34G>A
|
|
ENST00000545787.1:n.481+34G>A
|
|
|
ENST00000595085.5:c.853+34G>A
|
ENSP00000471150.2:n.853+34G>A
|
|
NM_000709.3:c.853+34G>A
|
NP_000700.1:n.853+34G>A
|
|
NM_001164783.1:c.853+34G>A
|
NP_001158255.1:n.853+34G>A
|
|
NM_000709.4:c.853+34G>A
MANE Select
|
NP_000700.1:n.853+34G>A
|
|
NM_001164783.2:c.853+34G>A
|
NP_001158255.1:n.853+34G>A
|
|