|
ENST00000395796.8:c.*1326A>C
|
ENSP00000379142.4:n.*1326A>C
|
|
|
ENST00000616242.5:c.*448A>C
|
ENSP00000482149.2:n.*448A>C
|
|
|
ENST00000683378.1:n.554A>C
|
|
|
|
ENST00000336642.9:c.362A>C
|
ENSP00000338009.5:p.Glu121Ala
|
|
|
ENST00000345378.7:c.1331A>C
|
ENSP00000223366.2:p.Glu444Ala
|
|
|
ENST00000403799.8:c.1328A>C
MANE Select
|
ENSP00000384247.3:p.Glu443Ala
|
|
|
ENST00000671824.1:c.1391A>C
|
ENSP00000500264.1:p.Glu464Ala
|
|
|
ENST00000672743.1:n.340A>C
|
|
|
|
ENST00000673284.1:c.1328A>C
|
ENSP00000499852.1:p.Glu443Ala
|
|
|
ENST00000336642.8:c.380A>C
|
ENSP00000338009.4:p.Glu127Ala
|
|
|
ENST00000345378.6:c.1331A>C
|
ENSP00000223366.2:p.Glu444Ala
|
|
|
ENST00000395796.7:c.1325A>C
|
ENSP00000379142.3:p.Glu442Ala
|
|
|
ENST00000403799.7:c.1328A>C
|
ENSP00000384247.3:p.Glu443Ala
|
|
|
ENST00000437084.1:c.1277A>C
|
ENSP00000402840.1:p.Glu426Ala
|
|
|
ENST00000459642.1:n.708A>C
|
|
|
|
ENST00000616242.4:c.1325A>C
|
ENSP00000482149.1:p.Glu442Ala
|
|
|
NM_000162.3:c.1328A>C
|
NP_000153.1:p.Glu443Ala
|
|
|
NM_033507.1:c.1331A>C
|
NP_277042.1:p.Glu444Ala
|
|
|
NM_033508.1:c.1325A>C
|
NP_277043.1:p.Glu442Ala
|
|
|
NM_000162.4:c.1328A>C
|
NP_000153.1:p.Glu443Ala
|
|
|
NM_001354800.1:c.1328A>C
|
NP_001341729.1:p.Glu443Ala
|
|
|
NM_001354801.1:c.317A>C
|
NP_001341730.1:p.Glu106Ala
|
|
|
NM_001354802.1:c.188A>C
|
NP_001341731.1:p.Glu63Ala
|
|
|
NM_001354803.1:c.362A>C
|
NP_001341732.1:p.Glu121Ala
|
|
|
NM_033507.2:c.1331A>C
|
NP_277042.1:p.Glu444Ala
|
|
|
NM_033508.2:c.1325A>C
|
NP_277043.1:p.Glu442Ala
|
|
|
XM_024446707.1:c.188A>C
|
XP_024302475.1:p.Glu63Ala
|
|
|
NM_000162.5:c.1328A>C
MANE Select
|
NP_000153.1:p.Glu443Ala
|
|
|
NM_033507.3:c.1331A>C
|
NP_277042.1:p.Glu444Ala
|
|
|
NM_033508.3:c.1325A>C
|
NP_277043.1:p.Glu442Ala
|
|
|
NM_001354803.2:c.362A>C
|
NP_001341732.1:p.Glu121Ala
|
|
