ENST00000398603.6:c.406G>C
|
ENSP00000381604.1:p.Asp136His
|
|
ENST00000398606.10:c.514G>C
MANE Select
|
ENSP00000381607.3:p.Asp172His
|
|
ENST00000646888.1:c.*230G>C
|
ENSP00000494477.1:n.*230G>C
|
|
ENST00000398603.5:c.406G>C
|
ENSP00000381604.1:p.Asp136His
|
|
ENST00000398606.7:c.514G>C
|
ENSP00000381607.3:p.Asp172His
|
|
ENST00000467591.1:n.625G>C
|
|
|
ENST00000494593.1:n.1486G>C
|
|
|
ENST00000498765.5:c.577G>C
|
|
|
NM_000852.3:c.514G>C , LRG_723t1:c.514G>C
|
NP_000843.1:p.Asp172His
|
|
NM_000852.4:c.514G>C
MANE Select
|
NP_000843.1:p.Asp172His
|
|