ENST00000398603.6:c.365A>T
|
ENSP00000381604.1:p.Asp122Val
|
|
ENST00000398606.10:c.473A>T
MANE Select
|
ENSP00000381607.3:p.Asp158Val
|
|
ENST00000646888.1:c.*189A>T
|
ENSP00000494477.1:n.*189A>T
|
|
ENST00000398603.5:c.365A>T
|
ENSP00000381604.1:p.Asp122Val
|
|
ENST00000398606.7:c.473A>T
|
ENSP00000381607.3:p.Asp158Val
|
|
ENST00000467591.1:n.584A>T
|
|
|
ENST00000494593.1:n.1445A>T
|
|
|
ENST00000495996.1:c.199A>T
|
ENSP00000484686.1:p.Thr67Ser
|
|
ENST00000498765.5:c.536A>T
|
|
|
NM_000852.3:c.473A>T , LRG_723t1:c.473A>T
|
NP_000843.1:p.Asp158Val
|
|
NM_000852.4:c.473A>T
MANE Select
|
NP_000843.1:p.Asp158Val
|
|