ENST00000398603.6:c.355A>C
|
ENSP00000381604.1:p.Asn119His
|
|
ENST00000398606.10:c.463A>C
MANE Select
|
ENSP00000381607.3:p.Asn155His
|
|
ENST00000646888.1:c.*179A>C
|
ENSP00000494477.1:n.*179A>C
|
|
ENST00000398603.5:c.355A>C
|
ENSP00000381604.1:p.Asn119His
|
|
ENST00000398606.7:c.463A>C
|
ENSP00000381607.3:p.Asn155His
|
|
ENST00000467591.1:n.574A>C
|
|
|
ENST00000494593.1:n.1435A>C
|
|
|
ENST00000495996.1:c.189A>C
|
ENSP00000484686.1:p.Thr63=
|
|
ENST00000498765.5:c.526A>C
|
|
|
NM_000852.3:c.463A>C , LRG_723t1:c.463A>C
|
NP_000843.1:p.Asn155His
|
|
NM_000852.4:c.463A>C
MANE Select
|
NP_000843.1:p.Asn155His
|
|