ENST00000398603.6:c.406G>T
|
ENSP00000381604.1:p.Asp136Tyr
|
|
ENST00000398606.10:c.514G>T
MANE Select
|
ENSP00000381607.3:p.Asp172Tyr
|
|
ENST00000646888.1:c.*230G>T
|
ENSP00000494477.1:n.*230G>T
|
|
ENST00000398603.5:c.406G>T
|
ENSP00000381604.1:p.Asp136Tyr
|
|
ENST00000398606.7:c.514G>T
|
ENSP00000381607.3:p.Asp172Tyr
|
|
ENST00000467591.1:n.625G>T
|
|
|
ENST00000494593.1:n.1486G>T
|
|
|
ENST00000498765.5:c.577G>T
|
|
|
NM_000852.3:c.514G>T , LRG_723t1:c.514G>T
|
NP_000843.1:p.Asp172Tyr
|
|
NM_000852.4:c.514G>T
MANE Select
|
NP_000843.1:p.Asp172Tyr
|
|