ENST00000398603.6:c.360G>T
|
ENSP00000381604.1:p.Leu120=
|
|
ENST00000398606.10:c.468G>T
MANE Select
|
ENSP00000381607.3:p.Leu156=
|
|
ENST00000646888.1:c.*184G>T
|
ENSP00000494477.1:n.*184G>T
|
|
ENST00000398603.5:c.360G>T
|
ENSP00000381604.1:p.Leu120=
|
|
ENST00000398606.7:c.468G>T
|
ENSP00000381607.3:p.Leu156=
|
|
ENST00000467591.1:n.579G>T
|
|
|
ENST00000494593.1:n.1440G>T
|
|
|
ENST00000495996.1:c.194G>T
|
ENSP00000484686.1:p.Cys65Phe
|
|
ENST00000498765.5:c.531G>T
|
|
|
NM_000852.3:c.468G>T , LRG_723t1:c.468G>T
|
NP_000843.1:p.Leu156=
|
|
NM_000852.4:c.468G>T
MANE Select
|
NP_000843.1:p.Leu156=
|
|