ENST00000263440.6:c.930T>A
MANE Select
|
ENSP00000263440.5:p.Leu310=
|
|
ENST00000603108.6:c.*79T>A
|
ENSP00000473934.2:n.*79T>A
|
|
ENST00000647818.1:c.*236T>A
|
ENSP00000497667.1:n.*236T>A
|
|
ENST00000648964.1:c.*659T>A
|
ENSP00000497828.1:n.*659T>A
|
|
ENST00000649570.1:c.*352T>A
|
ENSP00000497742.1:n.*352T>A
|
|
ENST00000650494.1:c.*287T>A
|
ENSP00000497170.1:n.*287T>A
|
|
ENST00000263440.4:c.936T>A
|
ENSP00000263440.4:p.Leu312=
|
|
ENST00000371108.8:c.930T>A
|
ENSP00000360149.4:p.Leu310=
|
|
ENST00000465969.5:n.519T>A
|
|
|
ENST00000603108.5:c.*8T>A
|
ENSP00000473934.1:n.*8T>A
|
|
NM_013339.3:c.930T>A
|
NP_037471.2:p.Leu310=
|
|
NM_013339.4:c.930T>A
MANE Select
|
NP_037471.2:p.Leu310=
|
|