ENST00000263440.6:c.919T>G
MANE Select
|
ENSP00000263440.5:p.Leu307Val
|
|
ENST00000603108.6:c.*68T>G
|
ENSP00000473934.2:n.*68T>G
|
|
ENST00000647818.1:c.*225T>G
|
ENSP00000497667.1:n.*225T>G
|
|
ENST00000648964.1:c.*648T>G
|
ENSP00000497828.1:n.*648T>G
|
|
ENST00000649570.1:c.*341T>G
|
ENSP00000497742.1:n.*341T>G
|
|
ENST00000650494.1:c.*276T>G
|
ENSP00000497170.1:n.*276T>G
|
|
ENST00000263440.4:c.925T>G
|
ENSP00000263440.4:p.Leu309Val
|
|
ENST00000371108.8:c.919T>G
|
ENSP00000360149.4:p.Leu307Val
|
|
ENST00000465969.5:n.508T>G
|
|
|
ENST00000603108.5:c.843T>G
|
ENSP00000473934.1:p.Phe281Leu
|
|
NM_013339.3:c.919T>G
|
NP_037471.2:p.Leu307Val
|
|
NM_013339.4:c.919T>G
MANE Select
|
NP_037471.2:p.Leu307Val
|
|