ENST00000398603.6:c.440G>A
|
ENSP00000381604.1:p.Arg147His
|
|
ENST00000398606.10:c.548G>A
MANE Select
|
ENSP00000381607.3:p.Arg183His
|
|
ENST00000646888.1:c.*264G>A
|
ENSP00000494477.1:n.*264G>A
|
|
ENST00000398603.5:c.440G>A
|
ENSP00000381604.1:p.Arg147His
|
|
ENST00000398606.7:c.548G>A
|
ENSP00000381607.3:p.Arg183His
|
|
ENST00000467591.1:n.659G>A
|
|
|
ENST00000494593.1:n.1520G>A
|
|
|
ENST00000498765.5:c.611G>A
|
|
|
NM_000852.3:c.548G>A , LRG_723t1:c.548G>A
|
NP_000843.1:p.Arg183His
|
|
NM_000852.4:c.548G>A
MANE Select
|
NP_000843.1:p.Arg183His
|
|