ENST00000698881.1:c.1188A>C
|
ENSP00000514003.1:p.Gly396=
|
|
ENST00000418331.7:c.846A>C
MANE Select
|
ENSP00000400010.2:p.Gly282=
|
|
ENST00000418331.6:c.846A>C
|
ENSP00000400010.2:p.Gly282=
|
|
ENST00000440289.6:c.846A>C
|
ENSP00000409733.2:p.Gly282=
|
|
ENST00000613246.4:c.846A>C
|
ENSP00000477933.1:p.Gly282=
|
|
ENST00000615445.4:c.846A>C
|
ENSP00000479342.1:p.Gly282=
|
|
NM_001098503.1:c.846A>C
|
NP_001091973.1:p.Gly282=
|
|
NM_002843.3:c.846A>C
|
NP_002834.3:p.Gly282=
|
|
XM_011520249.1:c.879A>C
|
XP_011518551.1:p.Gly293=
|
|
XR_930883.1:n.1196A>C
|
|
|
XM_017018083.1:c.924A>C
|
XP_016873572.1:p.Gly308=
|
|
XM_017018084.1:c.867A>C
|
XP_016873573.1:p.Gly289=
|
|
XM_017018085.1:c.798A>C
|
XP_016873574.1:p.Gly266=
|
|
XR_930883.2:n.1255A>C
|
|
|
NM_002843.4:c.846A>C
MANE Select
|
NP_002834.3:p.Gly282=
|
|
NM_001098503.2:c.846A>C
|
NP_001091973.1:p.Gly282=
|
|