ENST00000398603.6:c.439C>A
|
ENSP00000381604.1:p.Arg147Ser
|
|
ENST00000398606.10:c.547C>A
MANE Select
|
ENSP00000381607.3:p.Arg183Ser
|
|
ENST00000646888.1:c.*263C>A
|
ENSP00000494477.1:n.*263C>A
|
|
ENST00000398603.5:c.439C>A
|
ENSP00000381604.1:p.Arg147Ser
|
|
ENST00000398606.7:c.547C>A
|
ENSP00000381607.3:p.Arg183Ser
|
|
ENST00000467591.1:n.658C>A
|
|
|
ENST00000494593.1:n.1519C>A
|
|
|
ENST00000498765.5:c.610C>A
|
|
|
NM_000852.3:c.547C>A , LRG_723t1:c.547C>A
|
NP_000843.1:p.Arg183Ser
|
|
NM_000852.4:c.547C>A
MANE Select
|
NP_000843.1:p.Arg183Ser
|
|