|
ENST00000703936.1:c.2637A>C
|
ENSP00000515567.1:p.Glu879Asp
|
|
|
ENST00000703937.1:c.*1698A>C
|
ENSP00000515568.1:n.*1698A>C
|
|
|
ENST00000326739.9:c.597A>C
MANE Select
|
ENSP00000321584.4:p.Glu199Asp
|
|
|
ENST00000429182.6:c.597A>C
|
ENSP00000393525.2:p.Glu199Asp
|
|
|
ENST00000442157.2:c.522A>C
|
ENSP00000403502.2:p.Glu174Asp
|
|
|
ENST00000462980.2:n.1112A>C
|
|
|
|
ENST00000472328.2:n.663A>C
|
|
|
|
ENST00000491610.2:n.484A>C
|
|
|
|
ENST00000676607.1:n.893A>C
|
|
|
|
ENST00000676627.1:n.1327A>C
|
|
|
|
ENST00000676708.1:n.1804A>C
|
|
|
|
ENST00000676864.1:n.1673A>C
|
|
|
|
ENST00000677010.1:c.633A>C
|
ENSP00000503089.1:p.Glu211Asp
|
|
|
ENST00000677108.1:n.2430A>C
|
|
|
|
ENST00000677168.1:n.1069A>C
|
|
|
|
ENST00000677185.1:n.1087A>C
|
|
|
|
ENST00000677205.1:n.1308A>C
|
|
|
|
ENST00000677344.1:n.1798A>C
|
|
|
|
ENST00000677480.1:c.*274A>C
|
ENSP00000504378.1:n.*274A>C
|
|
|
ENST00000677519.1:n.1307A>C
|
|
|
|
ENST00000677593.1:n.1080A>C
|
|
|
|
ENST00000677740.1:n.2029A>C
|
|
|
|
ENST00000677991.1:n.1770A>C
|
|
|
|
ENST00000678001.1:n.1090A>C
|
|
|
|
ENST00000678085.1:n.1080A>C
|
|
|
|
ENST00000678177.1:n.2373A>C
|
|
|
|
ENST00000678603.1:n.1675A>C
|
|
|
|
ENST00000678724.1:c.522A>C
|
ENSP00000503874.1:p.Glu174Asp
|
|
|
ENST00000678920.1:n.755A>C
|
|
|
|
ENST00000679019.1:n.1294A>C
|
|
|
|
ENST00000679117.1:c.*412A>C
|
ENSP00000503240.1:n.*412A>C
|
|
|
ENST00000679339.1:n.1365A>C
|
|
|
|
ENST00000326739.8:c.597A>C
|
ENSP00000321584.4:p.Glu199Asp
|
|
|
ENST00000429182.5:c.391A>C
|
|
|
|
ENST00000442157.1:c.522A>C
|
ENSP00000403502.1:p.Glu174Asp
|
|
|
ENST00000462980.1:n.499A>C
|
|
|
|
ENST00000491610.1:n.484A>C
|
|
|
|
NM_000884.2:c.597A>C
|
NP_000875.2:p.Glu199Asp
|
|
|
XM_006713128.2:c.807A>C
|
XP_006713191.1:p.Glu269Asp
|
|
|
XM_006713128.3:c.807A>C
|
XP_006713191.1:p.Glu269Asp
|
|
|
XM_017006349.1:c.732A>C
|
XP_016861838.1:p.Glu244Asp
|
|
|
XM_017006350.1:c.732A>C
|
XP_016861839.1:p.Glu244Asp
|
|
|
NM_000884.3:c.597A>C
MANE Select
|
NP_000875.2:p.Glu199Asp
|
|
