ENST00000398603.6:c.401G>T
|
ENSP00000381604.1:p.Cys134Phe
|
|
ENST00000398606.10:c.509G>T
MANE Select
|
ENSP00000381607.3:p.Cys170Phe
|
|
ENST00000646888.1:c.*225G>T
|
ENSP00000494477.1:n.*225G>T
|
|
ENST00000398603.5:c.401G>T
|
ENSP00000381604.1:p.Cys134Phe
|
|
ENST00000398606.7:c.509G>T
|
ENSP00000381607.3:p.Cys170Phe
|
|
ENST00000467591.1:n.620G>T
|
|
|
ENST00000494593.1:n.1481G>T
|
|
|
ENST00000498765.5:c.572G>T
|
|
|
NM_000852.3:c.509G>T , LRG_723t1:c.509G>T
|
NP_000843.1:p.Cys170Phe
|
|
NM_000852.4:c.509G>T
MANE Select
|
NP_000843.1:p.Cys170Phe
|
|