ENST00000398603.6:c.358C>G
|
ENSP00000381604.1:p.Leu120Val
|
|
ENST00000398606.10:c.466C>G
MANE Select
|
ENSP00000381607.3:p.Leu156Val
|
|
ENST00000646888.1:c.*182C>G
|
ENSP00000494477.1:n.*182C>G
|
|
ENST00000398603.5:c.358C>G
|
ENSP00000381604.1:p.Leu120Val
|
|
ENST00000398606.7:c.466C>G
|
ENSP00000381607.3:p.Leu156Val
|
|
ENST00000467591.1:n.577C>G
|
|
|
ENST00000494593.1:n.1438C>G
|
|
|
ENST00000495996.1:c.192C>G
|
ENSP00000484686.1:p.Thr64=
|
|
ENST00000498765.5:c.529C>G
|
|
|
NM_000852.3:c.466C>G , LRG_723t1:c.466C>G
|
NP_000843.1:p.Leu156Val
|
|
NM_000852.4:c.466C>G
MANE Select
|
NP_000843.1:p.Leu156Val
|
|