ENST00000505026.2:c.2160A>G
|
ENSP00000516108.1:p.Glu720=
|
|
ENST00000691494.1:c.2643A>G
MANE Select
|
ENSP00000510694.1:p.Glu881=
|
|
ENST00000644474.1:c.2625A>G
|
ENSP00000495906.1:p.Glu875=
|
|
ENST00000644902.1:c.2289A>G
|
ENSP00000495298.1:p.Glu763=
|
|
ENST00000264431.8:c.2160A>G
|
ENSP00000264431.4:p.Glu720=
|
|
NM_014247.2:c.2160A>G
|
NP_055062.1:p.Glu720=
|
|
XM_005263358.2:c.2643A>G
|
XP_005263415.1:p.Glu881=
|
|
XM_005263359.2:c.2643A>G
|
XP_005263416.1:p.Glu881=
|
|
XM_005263360.2:c.2643A>G
|
XP_005263417.1:p.Glu881=
|
|
XM_005263361.2:c.2625A>G
|
XP_005263418.1:p.Glu875=
|
|
XM_006714420.2:c.2625A>G
|
XP_006714483.1:p.Glu875=
|
|
XM_006714421.2:c.2643A>G
|
XP_006714484.1:p.Glu881=
|
|
XM_006714422.2:c.2295A>G
|
XP_006714485.1:p.Glu765=
|
|
XM_011532425.1:c.2307A>G
|
XP_011530727.1:p.Glu769=
|
|
XM_011532426.1:c.2295A>G
|
XP_011530728.1:p.Glu765=
|
|
XM_011532427.1:c.2160A>G
|
XP_011530729.1:p.Glu720=
|
|
NM_001351724.1:c.2643A>G
|
NP_001338653.1:p.Glu881=
|
|
NM_001351725.1:c.2295A>G
|
NP_001338654.1:p.Glu765=
|
|
NM_001351726.1:c.2295A>G
|
NP_001338655.1:p.Glu765=
|
|
NM_001351727.1:c.2160A>G
|
NP_001338656.1:p.Glu720=
|
|
NM_001351728.1:c.2160A>G
|
NP_001338657.1:p.Glu720=
|
|
XM_005263358.3:c.2643A>G
|
XP_005263415.1:p.Glu881=
|
|
XM_005263359.4:c.2643A>G
|
XP_005263416.1:p.Glu881=
|
|
XM_005263360.3:c.2643A>G
|
XP_005263417.1:p.Glu881=
|
|
XM_005263361.3:c.2625A>G
|
XP_005263418.1:p.Glu875=
|
|
XM_006714420.3:c.2625A>G
|
XP_006714483.1:p.Glu875=
|
|
XM_006714422.4:c.2295A>G
|
XP_006714485.1:p.Glu765=
|
|
XM_011532425.2:c.2307A>G
|
XP_011530727.1:p.Glu769=
|
|
XM_011532426.2:c.2295A>G
|
XP_011530728.1:p.Glu765=
|
|
XM_017008856.2:c.2643A>G
|
XP_016864345.1:p.Glu881=
|
|
XM_024454286.1:c.2277A>G
|
XP_024310054.1:p.Glu759=
|
|
XM_024454287.1:c.2277A>G
|
XP_024310055.1:p.Glu759=
|
|
NM_001351724.2:c.2643A>G
|
NP_001338653.1:p.Glu881=
|
|
NM_001351727.2:c.2160A>G
|
NP_001338656.1:p.Glu720=
|
|
NM_001351728.2:c.2160A>G
|
NP_001338657.1:p.Glu720=
|
|
NM_014247.3:c.2160A>G
|
NP_055062.1:p.Glu720=
|
|
NM_001351724.4:c.2643A>G
|
NP_001338653.1:p.Glu881=
|
|
NM_001351725.2:c.2295A>G
|
NP_001338654.1:p.Glu765=
|
|
NM_001351726.3:c.2295A>G
|
NP_001338655.1:p.Glu765=
|
|
NM_001351727.4:c.2160A>G
|
NP_001338656.1:p.Glu720=
|
|
NM_001351728.4:c.2160A>G
|
NP_001338657.1:p.Glu720=
|
|
NM_001394067.1:c.2643A>G
|
NP_001380996.1:p.Glu881=
|
|
NM_014247.5:c.2160A>G
|
NP_055062.1:p.Glu720=
|
|
NM_001351724.5:c.2643A>G
|
NP_001338653.1:p.Glu881=
|
|
NM_001394067.2:c.2643A>G
MANE Select
|
NP_001380996.1:p.Glu881=
|
|