|
ENST00000703936.1:c.2691G>C
|
ENSP00000515567.1:p.Glu897Asp
|
|
|
ENST00000703937.1:c.*1752G>C
|
ENSP00000515568.1:n.*1752G>C
|
|
|
ENST00000326739.9:c.651G>C
MANE Select
|
ENSP00000321584.4:p.Glu217Asp
|
|
|
ENST00000429182.6:c.651G>C
|
ENSP00000393525.2:p.Glu217Asp
|
|
|
ENST00000442157.2:c.576G>C
|
ENSP00000403502.2:p.Glu192Asp
|
|
|
ENST00000462980.2:n.1166G>C
|
|
|
|
ENST00000472328.2:n.717G>C
|
|
|
|
ENST00000491610.2:n.611G>C
|
|
|
|
ENST00000676607.1:n.947G>C
|
|
|
|
ENST00000676627.1:n.1381G>C
|
|
|
|
ENST00000676708.1:n.1931G>C
|
|
|
|
ENST00000676864.1:n.1800G>C
|
|
|
|
ENST00000677010.1:c.687G>C
|
ENSP00000503089.1:p.Glu229Asp
|
|
|
ENST00000677108.1:n.2557G>C
|
|
|
|
ENST00000677168.1:n.1123G>C
|
|
|
|
ENST00000677185.1:n.1214G>C
|
|
|
|
ENST00000677205.1:n.1435G>C
|
|
|
|
ENST00000677344.1:n.1925G>C
|
|
|
|
ENST00000677480.1:c.*328G>C
|
ENSP00000504378.1:n.*328G>C
|
|
|
ENST00000677519.1:n.1361G>C
|
|
|
|
ENST00000677593.1:n.1207G>C
|
|
|
|
ENST00000677740.1:n.2156G>C
|
|
|
|
ENST00000677991.1:n.1824G>C
|
|
|
|
ENST00000678001.1:n.1144G>C
|
|
|
|
ENST00000678085.1:n.1207G>C
|
|
|
|
ENST00000678177.1:n.2500G>C
|
|
|
|
ENST00000678603.1:n.1729G>C
|
|
|
|
ENST00000678724.1:c.576G>C
|
ENSP00000503874.1:p.Glu192Asp
|
|
|
ENST00000678920.1:n.809G>C
|
|
|
|
ENST00000679019.1:n.1421G>C
|
|
|
|
ENST00000679117.1:c.*466G>C
|
ENSP00000503240.1:n.*466G>C
|
|
|
ENST00000679339.1:n.1492G>C
|
|
|
|
ENST00000326739.8:c.651G>C
|
ENSP00000321584.4:p.Glu217Asp
|
|
|
ENST00000429182.5:c.445G>C
|
|
|
|
ENST00000442157.1:c.576G>C
|
ENSP00000403502.1:p.Glu192Asp
|
|
|
ENST00000462980.1:n.553G>C
|
|
|
|
ENST00000491610.1:n.611G>C
|
|
|
|
NM_000884.2:c.651G>C
|
NP_000875.2:p.Glu217Asp
|
|
|
XM_006713128.2:c.861G>C
|
XP_006713191.1:p.Glu287Asp
|
|
|
XM_006713128.3:c.861G>C
|
XP_006713191.1:p.Glu287Asp
|
|
|
XM_017006349.1:c.786G>C
|
XP_016861838.1:p.Glu262Asp
|
|
|
XM_017006350.1:c.786G>C
|
XP_016861839.1:p.Glu262Asp
|
|
|
NM_000884.3:c.651G>C
MANE Select
|
NP_000875.2:p.Glu217Asp
|
|
