ENST00000398603.6:c.395C>A
|
ENSP00000381604.1:p.Pro132His
|
|
ENST00000398606.10:c.503C>A
MANE Select
|
ENSP00000381607.3:p.Pro168His
|
|
ENST00000646888.1:c.*219C>A
|
ENSP00000494477.1:n.*219C>A
|
|
ENST00000398603.5:c.395C>A
|
ENSP00000381604.1:p.Pro132His
|
|
ENST00000398606.7:c.503C>A
|
ENSP00000381607.3:p.Pro168His
|
|
ENST00000467591.1:n.614C>A
|
|
|
ENST00000494593.1:n.1475C>A
|
|
|
ENST00000498765.5:c.566C>A
|
|
|
NM_000852.3:c.503C>A , LRG_723t1:c.503C>A
|
NP_000843.1:p.Pro168His
|
|
NM_000852.4:c.503C>A
MANE Select
|
NP_000843.1:p.Pro168His
|
|