ENST00000269980.7:c.996-14T>G
MANE Select
|
ENSP00000269980.2:n.996-14T>G
|
|
ENST00000269980.6:c.996-14T>G
|
ENSP00000269980.2:n.996-14T>G
|
|
ENST00000457836.6:c.991T>G
|
ENSP00000416000.2:p.Leu331Val
|
|
ENST00000540732.3:c.1098-14T>G
|
ENSP00000443246.1:n.1098-14T>G
|
|
ENST00000542943.5:c.909-14T>G
|
ENSP00000440345.1:n.909-14T>G
|
|
ENST00000595085.5:c.922+287T>G
|
ENSP00000471150.2:n.922+287T>G
|
|
NM_000709.3:c.996-14T>G
|
NP_000700.1:n.996-14T>G
|
|
NM_001164783.1:c.993-14T>G
|
NP_001158255.1:n.993-14T>G
|
|
NM_000709.4:c.996-14T>G
MANE Select
|
NP_000700.1:n.996-14T>G
|
|
NM_001164783.2:c.993-14T>G
|
NP_001158255.1:n.993-14T>G
|
|