ENST00000263038.9:c.817G=
MANE Select
|
ENSP00000263038.4:p.Gly273=
|
|
ENST00000263038.8:c.817G=
|
ENSP00000263038.4:p.Gly273=
|
|
ENST00000396913.6:c.517G=
|
ENSP00000380121.2:p.Gly173=
|
|
ENST00000396920.7:c.766G=
|
ENSP00000380126.3:p.Gly256=
|
|
ENST00000453759.6:c.517G=
|
ENSP00000412525.2:p.Gly173=
|
|
NM_001037537.1:c.517G=
|
NP_001032626.1:p.Gly173=
|
|
NM_006214.3:c.817G=
|
NP_006205.1:p.Gly273=
|
|
XM_005252469.2:c.598G=
|
XP_005252526.1:p.Gly200=
|
|
NM_001323080.1:c.517G=
|
NP_001310009.1:p.Gly173=
|
|
NM_001323082.1:c.823G=
|
NP_001310011.1:p.Gly275=
|
|
NM_001323083.1:c.553G=
|
NP_001310012.1:p.Gly185=
|
|
NM_001323084.1:c.523G=
|
NP_001310013.1:p.Gly175=
|
|
NM_006214.4:c.817G=
MANE Select
|
NP_006205.1:p.Gly273=
|
|
NM_001037537.2:c.517G=
|
NP_001032626.1:p.Gly173=
|
|
NM_001323080.2:c.517G=
|
NP_001310009.1:p.Gly173=
|
|
NM_001323082.2:c.823G=
|
NP_001310011.1:p.Gly275=
|
|
NM_001323083.2:c.553G=
|
NP_001310012.1:p.Gly185=
|
|
NM_001323084.2:c.523G=
|
NP_001310013.1:p.Gly175=
|
|