ENST00000296589.9:c.850G=
MANE Select
|
ENSP00000296589.4:p.Ala284=
|
|
ENST00000296589.8:c.850G=
|
ENSP00000296589.4:p.Ala284=
|
|
ENST00000382102.7:c.850G=
|
ENSP00000371534.3:p.Ala284=
|
|
ENST00000505056.1:n.652G=
|
|
|
ENST00000509381.1:c.563-9225G=
|
ENSP00000421100.1:n.563-9225G=
|
|
ENST00000510600.1:c.325G=
|
ENSP00000424010.1:p.Ala109=
|
|
NM_001012509.3:c.850G=
|
NP_001012527.1:p.Ala284=
|
|
NM_001297417.2:c.563-9225G=
|
NP_001284346.2:n.563-9225G=
|
|
NM_016180.4:c.850G=
|
NP_057264.3:p.Ala284=
|
|
XM_011514051.1:c.448G=
|
XP_011512353.1:p.Ala150=
|
|
XM_011514052.1:c.850G=
|
XP_011512354.1:p.Ala284=
|
|
XR_925620.1:n.1667G=
|
|
|
NM_016180.5:c.850G=
MANE Select
|
NP_057264.4:p.Ala284=
|
|
NM_001012509.4:c.850G=
|
NP_001012527.2:p.Ala284=
|
|
NM_001297417.3:c.563-9225G=
|
NP_001284346.2:n.563-9225G=
|
|
NM_001297417.4:c.563-9225G=
|
NP_001284346.2:n.563-9225G=
|
|