ENST00000398603.6:c.364G>C
|
ENSP00000381604.1:p.Asp122His
|
|
ENST00000398606.10:c.472G>C
MANE Select
|
ENSP00000381607.3:p.Asp158His
|
|
ENST00000646888.1:c.*188G>C
|
ENSP00000494477.1:n.*188G>C
|
|
ENST00000398603.5:c.364G>C
|
ENSP00000381604.1:p.Asp122His
|
|
ENST00000398606.7:c.472G>C
|
ENSP00000381607.3:p.Asp158His
|
|
ENST00000467591.1:n.583G>C
|
|
|
ENST00000494593.1:n.1444G>C
|
|
|
ENST00000495996.1:c.198G>C
|
ENSP00000484686.1:p.Trp66Cys
|
|
ENST00000498765.5:c.535G>C
|
|
|
NM_000852.3:c.472G>C , LRG_723t1:c.472G>C
|
NP_000843.1:p.Asp158His
|
|
NM_000852.4:c.472G>C
MANE Select
|
NP_000843.1:p.Asp158His
|
|