|
ENST00000703936.1:c.2680G>C
|
ENSP00000515567.1:p.Glu894Gln
|
|
|
ENST00000703937.1:c.*1741G>C
|
ENSP00000515568.1:n.*1741G>C
|
|
|
ENST00000326739.9:c.640G>C
MANE Select
|
ENSP00000321584.4:p.Glu214Gln
|
|
|
ENST00000429182.6:c.640G>C
|
ENSP00000393525.2:p.Glu214Gln
|
|
|
ENST00000442157.2:c.565G>C
|
ENSP00000403502.2:p.Glu189Gln
|
|
|
ENST00000462980.2:n.1155G>C
|
|
|
|
ENST00000472328.2:n.706G>C
|
|
|
|
ENST00000491610.2:n.600G>C
|
|
|
|
ENST00000676607.1:n.936G>C
|
|
|
|
ENST00000676627.1:n.1370G>C
|
|
|
|
ENST00000676708.1:n.1920G>C
|
|
|
|
ENST00000676864.1:n.1789G>C
|
|
|
|
ENST00000677010.1:c.676G>C
|
ENSP00000503089.1:p.Glu226Gln
|
|
|
ENST00000677108.1:n.2546G>C
|
|
|
|
ENST00000677168.1:n.1112G>C
|
|
|
|
ENST00000677185.1:n.1203G>C
|
|
|
|
ENST00000677205.1:n.1424G>C
|
|
|
|
ENST00000677344.1:n.1914G>C
|
|
|
|
ENST00000677480.1:c.*317G>C
|
ENSP00000504378.1:n.*317G>C
|
|
|
ENST00000677519.1:n.1350G>C
|
|
|
|
ENST00000677593.1:n.1196G>C
|
|
|
|
ENST00000677740.1:n.2145G>C
|
|
|
|
ENST00000677991.1:n.1813G>C
|
|
|
|
ENST00000678001.1:n.1133G>C
|
|
|
|
ENST00000678085.1:n.1196G>C
|
|
|
|
ENST00000678177.1:n.2489G>C
|
|
|
|
ENST00000678603.1:n.1718G>C
|
|
|
|
ENST00000678724.1:c.565G>C
|
ENSP00000503874.1:p.Glu189Gln
|
|
|
ENST00000678920.1:n.798G>C
|
|
|
|
ENST00000679019.1:n.1410G>C
|
|
|
|
ENST00000679117.1:c.*455G>C
|
ENSP00000503240.1:n.*455G>C
|
|
|
ENST00000679339.1:n.1481G>C
|
|
|
|
ENST00000326739.8:c.640G>C
|
ENSP00000321584.4:p.Glu214Gln
|
|
|
ENST00000429182.5:c.434G>C
|
|
|
|
ENST00000442157.1:c.565G>C
|
ENSP00000403502.1:p.Glu189Gln
|
|
|
ENST00000462980.1:n.542G>C
|
|
|
|
ENST00000491610.1:n.600G>C
|
|
|
|
NM_000884.2:c.640G>C
|
NP_000875.2:p.Glu214Gln
|
|
|
XM_006713128.2:c.850G>C
|
XP_006713191.1:p.Glu284Gln
|
|
|
XM_006713128.3:c.850G>C
|
XP_006713191.1:p.Glu284Gln
|
|
|
XM_017006349.1:c.775G>C
|
XP_016861838.1:p.Glu259Gln
|
|
|
XM_017006350.1:c.775G>C
|
XP_016861839.1:p.Glu259Gln
|
|
|
NM_000884.3:c.640G>C
MANE Select
|
NP_000875.2:p.Glu214Gln
|
|
