ENST00000269980.7:c.995+112T>C
MANE Select
|
ENSP00000269980.2:n.995+112T>C
|
|
ENST00000269980.6:c.995+112T>C
|
ENSP00000269980.2:n.995+112T>C
|
|
ENST00000457836.6:c.930-41T>C
|
ENSP00000416000.2:n.930-41T>C
|
|
ENST00000540732.3:c.1097+112T>C
|
ENSP00000443246.1:n.1097+112T>C
|
|
ENST00000542943.5:c.908+112T>C
|
ENSP00000440345.1:n.908+112T>C
|
|
ENST00000595085.5:c.922+185T>C
|
ENSP00000471150.2:n.922+185T>C
|
|
NM_000709.3:c.995+112T>C
|
NP_000700.1:n.995+112T>C
|
|
NM_001164783.1:c.992+112T>C
|
NP_001158255.1:n.992+112T>C
|
|
NM_000709.4:c.995+112T>C
MANE Select
|
NP_000700.1:n.995+112T>C
|
|
NM_001164783.2:c.992+112T>C
|
NP_001158255.1:n.992+112T>C
|
|