ENST00000330889.8:c.1061A=
MANE Select
|
ENSP00000329468.3:p.Glu354=
|
|
ENST00000330889.7:c.1061A=
|
ENSP00000329468.3:p.Glu354=
|
|
ENST00000470962.1:n.481A=
|
|
|
ENST00000480980.1:n.495A=
|
|
|
ENST00000580525.5:c.1079A=
|
ENSP00000464121.1:p.Glu360=
|
|
ENST00000581285.5:c.977A=
|
ENSP00000464155.1:p.Glu326=
|
|
ENST00000584828.5:c.402+28A=
|
|
|
ENST00000585130.5:c.*660A=
|
ENSP00000464120.1:n.*660A=
|
|
NM_018404.2:c.1061A=
|
NP_060874.1:p.Glu354=
|
|
XM_005258008.2:c.1079A=
|
XP_005258065.1:p.Glu360=
|
|
XM_005258011.2:c.1016A=
|
XP_005258068.1:p.Glu339=
|
|
XM_006721973.2:c.1051+28A=
|
XP_006722036.1:n.1051+28A=
|
|
XM_011524993.1:c.1076A=
|
XP_011523295.1:p.Glu359=
|
|
XM_011524994.1:c.1058A=
|
XP_011523296.1:p.Glu353=
|
|
NM_001346712.1:c.1079A=
|
NP_001333641.1:p.Glu360=
|
|
NM_001346714.1:c.1058A=
|
NP_001333643.1:p.Glu353=
|
|
NM_001346716.1:c.1033+28A=
|
NP_001333645.1:n.1033+28A=
|
|
NR_144488.1:n.1260A=
|
|
|
XM_024450831.1:c.1061A=
|
XP_024306599.1:p.Glu354=
|
|
XM_024450832.1:c.1076A=
|
XP_024306600.1:p.Glu359=
|
|
XM_024450833.1:c.1016A=
|
XP_024306601.1:p.Glu339=
|
|
XM_024450834.1:c.1051+28A=
|
XP_024306602.1:n.1051+28A=
|
|
XM_024450835.1:c.695A=
|
XP_024306603.1:p.Glu232=
|
|
NM_018404.3:c.1061A=
MANE Select
|
NP_060874.1:p.Glu354=
|
|
NM_001346712.2:c.1079A=
|
NP_001333641.1:p.Glu360=
|
|
NM_001346714.2:c.1058A=
|
NP_001333643.1:p.Glu353=
|
|
NM_001346716.2:c.1033+28A=
|
NP_001333645.1:n.1033+28A=
|
|
NR_144488.2:n.1051A=
|
|
|