ENST00000398603.6:c.373C>G
|
ENSP00000381604.1:p.Leu125Val
|
|
ENST00000398606.10:c.481C>G
MANE Select
|
ENSP00000381607.3:p.Leu161Val
|
|
ENST00000646888.1:c.*197C>G
|
ENSP00000494477.1:n.*197C>G
|
|
ENST00000398603.5:c.373C>G
|
ENSP00000381604.1:p.Leu125Val
|
|
ENST00000398606.7:c.481C>G
|
ENSP00000381607.3:p.Leu161Val
|
|
ENST00000467591.1:n.592C>G
|
|
|
ENST00000494593.1:n.1453C>G
|
|
|
ENST00000495996.1:c.207C>G
|
ENSP00000484686.1:p.Cys69Trp
|
|
ENST00000498765.5:c.544C>G
|
|
|
NM_000852.3:c.481C>G , LRG_723t1:c.481C>G
|
NP_000843.1:p.Leu161Val
|
|
NM_000852.4:c.481C>G
MANE Select
|
NP_000843.1:p.Leu161Val
|
|