ENST00000336098.8:c.*125G>T
MANE Select
|
ENSP00000336829.3:n.*125G>T
|
|
ENST00000336098.7:c.*125G>T
|
ENSP00000336829.3:n.*125G>T
|
|
ENST00000404648.7:c.1299+188G>T
|
ENSP00000384860.3:n.1299+188G>T
|
|
ENST00000405164.5:c.1323+188G>T
|
ENSP00000384101.1:n.1323+188G>T
|
|
ENST00000407946.5:c.*125G>T
|
ENSP00000384552.1:n.*125G>T
|
|
ENST00000465913.1:n.1035G>T
|
|
|
ENST00000492082.5:n.1841+188G>T
|
|
|
NM_000509.4:c.1299+188G>T
|
NP_000500.2:n.1299+188G>T
|
|
NM_000509.5:c.1299+188G>T
|
NP_000500.2:n.1299+188G>T
|
|
NM_021870.2:c.*125G>T
|
NP_068656.2:n.*125G>T
|
|
NM_021870.3:c.*125G>T
MANE Select
|
NP_068656.2:n.*125G>T
|
|
NM_000509.6:c.1299+188G>T
|
NP_000500.2:n.1299+188G>T
|
|