ENST00000398603.6:c.439C>T
|
ENSP00000381604.1:p.Arg147Cys
|
|
ENST00000398606.10:c.547C>T
MANE Select
|
ENSP00000381607.3:p.Arg183Cys
|
|
ENST00000646888.1:c.*263C>T
|
ENSP00000494477.1:n.*263C>T
|
|
ENST00000398603.5:c.439C>T
|
ENSP00000381604.1:p.Arg147Cys
|
|
ENST00000398606.7:c.547C>T
|
ENSP00000381607.3:p.Arg183Cys
|
|
ENST00000467591.1:n.658C>T
|
|
|
ENST00000494593.1:n.1519C>T
|
|
|
ENST00000498765.5:c.610C>T
|
|
|
NM_000852.3:c.547C>T , LRG_723t1:c.547C>T
|
NP_000843.1:p.Arg183Cys
|
|
NM_000852.4:c.547C>T
MANE Select
|
NP_000843.1:p.Arg183Cys
|
|