ENST00000395796.8:c.*1013G=
|
ENSP00000379142.4:n.*1013G=
|
|
ENST00000616242.5:c.*135G=
|
ENSP00000482149.2:n.*135G=
|
|
ENST00000683378.1:n.241G=
|
|
|
ENST00000345378.7:c.1018G=
|
ENSP00000223366.2:p.Glu340=
|
|
ENST00000403799.8:c.1015G=
MANE Select
|
ENSP00000384247.3:p.Glu339=
|
|
ENST00000671824.1:c.1078G=
|
ENSP00000500264.1:p.Glu360=
|
|
ENST00000673284.1:c.1015G=
|
ENSP00000499852.1:p.Glu339=
|
|
ENST00000345378.6:c.1018G=
|
ENSP00000223366.2:p.Glu340=
|
|
ENST00000395796.7:c.1012G=
|
ENSP00000379142.3:p.Glu338=
|
|
ENST00000403799.7:c.1015G=
|
ENSP00000384247.3:p.Glu339=
|
|
ENST00000437084.1:c.964G=
|
ENSP00000402840.1:p.Glu322=
|
|
ENST00000473353.1:n.313G=
|
|
|
ENST00000616242.4:c.1012G=
|
ENSP00000482149.1:p.Glu338=
|
|
NM_000162.3:c.1015G=
|
NP_000153.1:p.Glu339=
|
|
NM_033507.1:c.1018G=
|
NP_277042.1:p.Glu340=
|
|
NM_033508.1:c.1012G=
|
NP_277043.1:p.Glu338=
|
|
NM_000162.4:c.1015G=
|
NP_000153.1:p.Glu339=
|
|
NM_001354800.1:c.1015G=
|
NP_001341729.1:p.Glu339=
|
|
NM_001354801.1:c.8+152G=
|
NP_001341730.1:n.8+152G=
|
|
NM_033507.2:c.1018G=
|
NP_277042.1:p.Glu340=
|
|
NM_033508.2:c.1012G=
|
NP_277043.1:p.Glu338=
|
|
NM_000162.5:c.1015G=
MANE Select
|
NP_000153.1:p.Glu339=
|
|
NM_033507.3:c.1018G=
|
NP_277042.1:p.Glu340=
|
|
NM_033508.3:c.1012G=
|
NP_277043.1:p.Glu338=
|
|