ENST00000299565.9:c.1234G>C
MANE Select
|
ENSP00000299565.5:p.Asp412His
|
|
ENST00000394802.4:c.522+527G>C
|
|
|
ENST00000559554.5:c.458+776G>C
|
ENSP00000453519.1:n.458+776G>C
|
|
ENST00000559576.1:c.145+119G>C
|
|
|
NM_000745.3:c.1234G>C
|
NP_000736.2:p.Asp412His
|
|
NM_001307945.1:c.458+776G>C
|
NP_001294874.1:n.458+776G>C
|
|
XM_005254142.2:c.707+527G>C
|
XP_005254199.1:n.707+527G>C
|
|
NM_001307945.2:c.458+776G>C
|
NP_001294874.1:n.458+776G>C
|
|
NM_000745.4:c.1234G>C
MANE Select
|
NP_000736.2:p.Asp412His
|
|
NM_001395171.1:c.1115+119G>C
|
NP_001382100.1:n.1115+119G>C
|
|
NM_001395172.1:c.591+643G>C
|
NP_001382101.1:n.591+643G>C
|
|
NM_001395173.1:c.713+521G>C
|
NP_001382102.1:n.713+521G>C
|
|
NM_001395174.1:c.707+527G>C
|
NP_001382103.1:n.707+527G>C
|
|
NM_001395175.1:c.455+776G>C
|
NP_001382104.1:n.455+776G>C
|
|