ENST00000398603.6:c.413T>G
|
ENSP00000381604.1:p.Phe138Cys
|
|
ENST00000398606.10:c.521T>G
MANE Select
|
ENSP00000381607.3:p.Phe174Cys
|
|
ENST00000646888.1:c.*237T>G
|
ENSP00000494477.1:n.*237T>G
|
|
ENST00000398603.5:c.413T>G
|
ENSP00000381604.1:p.Phe138Cys
|
|
ENST00000398606.7:c.521T>G
|
ENSP00000381607.3:p.Phe174Cys
|
|
ENST00000467591.1:n.632T>G
|
|
|
ENST00000494593.1:n.1493T>G
|
|
|
ENST00000498765.5:c.584T>G
|
|
|
NM_000852.3:c.521T>G , LRG_723t1:c.521T>G
|
NP_000843.1:p.Phe174Cys
|
|
NM_000852.4:c.521T>G
MANE Select
|
NP_000843.1:p.Phe174Cys
|
|