|
ENST00000703936.1:c.2681A>C
|
ENSP00000515567.1:p.Glu894Ala
|
|
|
ENST00000703937.1:c.*1742A>C
|
ENSP00000515568.1:n.*1742A>C
|
|
|
ENST00000326739.9:c.641A>C
MANE Select
|
ENSP00000321584.4:p.Glu214Ala
|
|
|
ENST00000429182.6:c.641A>C
|
ENSP00000393525.2:p.Glu214Ala
|
|
|
ENST00000442157.2:c.566A>C
|
ENSP00000403502.2:p.Glu189Ala
|
|
|
ENST00000462980.2:n.1156A>C
|
|
|
|
ENST00000472328.2:n.707A>C
|
|
|
|
ENST00000491610.2:n.601A>C
|
|
|
|
ENST00000676607.1:n.937A>C
|
|
|
|
ENST00000676627.1:n.1371A>C
|
|
|
|
ENST00000676708.1:n.1921A>C
|
|
|
|
ENST00000676864.1:n.1790A>C
|
|
|
|
ENST00000677010.1:c.677A>C
|
ENSP00000503089.1:p.Glu226Ala
|
|
|
ENST00000677108.1:n.2547A>C
|
|
|
|
ENST00000677168.1:n.1113A>C
|
|
|
|
ENST00000677185.1:n.1204A>C
|
|
|
|
ENST00000677205.1:n.1425A>C
|
|
|
|
ENST00000677344.1:n.1915A>C
|
|
|
|
ENST00000677480.1:c.*318A>C
|
ENSP00000504378.1:n.*318A>C
|
|
|
ENST00000677519.1:n.1351A>C
|
|
|
|
ENST00000677593.1:n.1197A>C
|
|
|
|
ENST00000677740.1:n.2146A>C
|
|
|
|
ENST00000677991.1:n.1814A>C
|
|
|
|
ENST00000678001.1:n.1134A>C
|
|
|
|
ENST00000678085.1:n.1197A>C
|
|
|
|
ENST00000678177.1:n.2490A>C
|
|
|
|
ENST00000678603.1:n.1719A>C
|
|
|
|
ENST00000678724.1:c.566A>C
|
ENSP00000503874.1:p.Glu189Ala
|
|
|
ENST00000678920.1:n.799A>C
|
|
|
|
ENST00000679019.1:n.1411A>C
|
|
|
|
ENST00000679117.1:c.*456A>C
|
ENSP00000503240.1:n.*456A>C
|
|
|
ENST00000679339.1:n.1482A>C
|
|
|
|
ENST00000326739.8:c.641A>C
|
ENSP00000321584.4:p.Glu214Ala
|
|
|
ENST00000429182.5:c.435A>C
|
|
|
|
ENST00000442157.1:c.566A>C
|
ENSP00000403502.1:p.Glu189Ala
|
|
|
ENST00000462980.1:n.543A>C
|
|
|
|
ENST00000491610.1:n.601A>C
|
|
|
|
NM_000884.2:c.641A>C
|
NP_000875.2:p.Glu214Ala
|
|
|
XM_006713128.2:c.851A>C
|
XP_006713191.1:p.Glu284Ala
|
|
|
XM_006713128.3:c.851A>C
|
XP_006713191.1:p.Glu284Ala
|
|
|
XM_017006349.1:c.776A>C
|
XP_016861838.1:p.Glu259Ala
|
|
|
XM_017006350.1:c.776A>C
|
XP_016861839.1:p.Glu259Ala
|
|
|
NM_000884.3:c.641A>C
MANE Select
|
NP_000875.2:p.Glu214Ala
|
|
