ENST00000398603.6:c.367T>G
|
ENSP00000381604.1:p.Leu123Val
|
|
ENST00000398606.10:c.475T>G
MANE Select
|
ENSP00000381607.3:p.Leu159Val
|
|
ENST00000646888.1:c.*191T>G
|
ENSP00000494477.1:n.*191T>G
|
|
ENST00000398603.5:c.367T>G
|
ENSP00000381604.1:p.Leu123Val
|
|
ENST00000398606.7:c.475T>G
|
ENSP00000381607.3:p.Leu159Val
|
|
ENST00000467591.1:n.586T>G
|
|
|
ENST00000494593.1:n.1447T>G
|
|
|
ENST00000495996.1:c.201T>G
|
ENSP00000484686.1:p.Thr67=
|
|
ENST00000498765.5:c.538T>G
|
|
|
NM_000852.3:c.475T>G , LRG_723t1:c.475T>G
|
NP_000843.1:p.Leu159Val
|
|
NM_000852.4:c.475T>G
MANE Select
|
NP_000843.1:p.Leu159Val
|
|