|
ENST00000703936.1:c.2626G>C
|
ENSP00000515567.1:p.Glu876Gln
|
|
|
ENST00000703937.1:c.*1687G>C
|
ENSP00000515568.1:n.*1687G>C
|
|
|
ENST00000326739.9:c.586G>C
MANE Select
|
ENSP00000321584.4:p.Glu196Gln
|
|
|
ENST00000429182.6:c.586G>C
|
ENSP00000393525.2:p.Glu196Gln
|
|
|
ENST00000442157.2:c.511G>C
|
ENSP00000403502.2:p.Glu171Gln
|
|
|
ENST00000462980.2:n.1101G>C
|
|
|
|
ENST00000472328.2:n.652G>C
|
|
|
|
ENST00000491610.2:n.473G>C
|
|
|
|
ENST00000676607.1:n.882G>C
|
|
|
|
ENST00000676627.1:n.1316G>C
|
|
|
|
ENST00000676708.1:n.1793G>C
|
|
|
|
ENST00000676864.1:n.1662G>C
|
|
|
|
ENST00000677010.1:c.622G>C
|
ENSP00000503089.1:p.Glu208Gln
|
|
|
ENST00000677108.1:n.2419G>C
|
|
|
|
ENST00000677168.1:n.1058G>C
|
|
|
|
ENST00000677185.1:n.1076G>C
|
|
|
|
ENST00000677205.1:n.1297G>C
|
|
|
|
ENST00000677344.1:n.1787G>C
|
|
|
|
ENST00000677480.1:c.*263G>C
|
ENSP00000504378.1:n.*263G>C
|
|
|
ENST00000677519.1:n.1296G>C
|
|
|
|
ENST00000677593.1:n.1069G>C
|
|
|
|
ENST00000677740.1:n.2018G>C
|
|
|
|
ENST00000677991.1:n.1759G>C
|
|
|
|
ENST00000678001.1:n.1079G>C
|
|
|
|
ENST00000678085.1:n.1069G>C
|
|
|
|
ENST00000678177.1:n.2362G>C
|
|
|
|
ENST00000678603.1:n.1664G>C
|
|
|
|
ENST00000678724.1:c.511G>C
|
ENSP00000503874.1:p.Glu171Gln
|
|
|
ENST00000678920.1:n.744G>C
|
|
|
|
ENST00000679019.1:n.1283G>C
|
|
|
|
ENST00000679117.1:c.*401G>C
|
ENSP00000503240.1:n.*401G>C
|
|
|
ENST00000679339.1:n.1354G>C
|
|
|
|
ENST00000326739.8:c.586G>C
|
ENSP00000321584.4:p.Glu196Gln
|
|
|
ENST00000429182.5:c.380G>C
|
|
|
|
ENST00000442157.1:c.511G>C
|
ENSP00000403502.1:p.Glu171Gln
|
|
|
ENST00000462980.1:n.488G>C
|
|
|
|
ENST00000491610.1:n.473G>C
|
|
|
|
NM_000884.2:c.586G>C
|
NP_000875.2:p.Glu196Gln
|
|
|
XM_006713128.2:c.796G>C
|
XP_006713191.1:p.Glu266Gln
|
|
|
XM_006713128.3:c.796G>C
|
XP_006713191.1:p.Glu266Gln
|
|
|
XM_017006349.1:c.721G>C
|
XP_016861838.1:p.Glu241Gln
|
|
|
XM_017006350.1:c.721G>C
|
XP_016861839.1:p.Glu241Gln
|
|
|
NM_000884.3:c.586G>C
MANE Select
|
NP_000875.2:p.Glu196Gln
|
|
