ENST00000379727.8:c.1276G=
MANE Select
|
ENSP00000369050.3:p.Glu426=
|
|
ENST00000379727.7:c.1276G=
|
ENSP00000369050.3:p.Glu426=
|
|
ENST00000395048.6:c.1276G=
|
ENSP00000378488.2:p.Glu426=
|
|
ENST00000395049.8:c.1189G=
|
ENSP00000378489.4:p.Glu397=
|
|
ENST00000562201.5:c.*513G=
|
ENSP00000455340.1:n.*513G=
|
|
ENST00000564596.5:c.*211G=
|
ENSP00000457668.1:n.*211G=
|
|
ENST00000566503.1:c.493G=
|
ENSP00000455846.1:p.Glu165=
|
|
ENST00000567032.5:c.1276G=
|
ENSP00000456585.1:p.Glu426=
|
|
ENST00000569630.5:c.*865G=
|
ENSP00000455051.1:n.*865G=
|
|
ENST00000612821.4:c.1192G=
|
ENSP00000479744.1:p.Glu398=
|
|
ENST00000617691.4:c.1189G=
|
ENSP00000482863.1:p.Glu397=
|
|
NM_000499.3:c.1276G=
|
NP_000490.1:p.Glu426=
|
|
XM_005254185.1:c.1276G=
|
XP_005254242.1:p.Glu426=
|
|
NM_000499.5:c.1276G=
|
NP_000490.1:p.Glu426=
|
|
NM_001319216.2:c.1189G=
|
NP_001306145.1:p.Glu397=
|
|
NM_001319217.2:c.1276G=
MANE Select
|
NP_001306146.1:p.Glu426=
|
|