|
ENST00000703936.1:c.2627A>C
|
ENSP00000515567.1:p.Glu876Ala
|
|
|
ENST00000703937.1:c.*1688A>C
|
ENSP00000515568.1:n.*1688A>C
|
|
|
ENST00000326739.9:c.587A>C
MANE Select
|
ENSP00000321584.4:p.Glu196Ala
|
|
|
ENST00000429182.6:c.587A>C
|
ENSP00000393525.2:p.Glu196Ala
|
|
|
ENST00000442157.2:c.512A>C
|
ENSP00000403502.2:p.Glu171Ala
|
|
|
ENST00000462980.2:n.1102A>C
|
|
|
|
ENST00000472328.2:n.653A>C
|
|
|
|
ENST00000491610.2:n.474A>C
|
|
|
|
ENST00000676607.1:n.883A>C
|
|
|
|
ENST00000676627.1:n.1317A>C
|
|
|
|
ENST00000676708.1:n.1794A>C
|
|
|
|
ENST00000676864.1:n.1663A>C
|
|
|
|
ENST00000677010.1:c.623A>C
|
ENSP00000503089.1:p.Glu208Ala
|
|
|
ENST00000677108.1:n.2420A>C
|
|
|
|
ENST00000677168.1:n.1059A>C
|
|
|
|
ENST00000677185.1:n.1077A>C
|
|
|
|
ENST00000677205.1:n.1298A>C
|
|
|
|
ENST00000677344.1:n.1788A>C
|
|
|
|
ENST00000677480.1:c.*264A>C
|
ENSP00000504378.1:n.*264A>C
|
|
|
ENST00000677519.1:n.1297A>C
|
|
|
|
ENST00000677593.1:n.1070A>C
|
|
|
|
ENST00000677740.1:n.2019A>C
|
|
|
|
ENST00000677991.1:n.1760A>C
|
|
|
|
ENST00000678001.1:n.1080A>C
|
|
|
|
ENST00000678085.1:n.1070A>C
|
|
|
|
ENST00000678177.1:n.2363A>C
|
|
|
|
ENST00000678603.1:n.1665A>C
|
|
|
|
ENST00000678724.1:c.512A>C
|
ENSP00000503874.1:p.Glu171Ala
|
|
|
ENST00000678920.1:n.745A>C
|
|
|
|
ENST00000679019.1:n.1284A>C
|
|
|
|
ENST00000679117.1:c.*402A>C
|
ENSP00000503240.1:n.*402A>C
|
|
|
ENST00000679339.1:n.1355A>C
|
|
|
|
ENST00000326739.8:c.587A>C
|
ENSP00000321584.4:p.Glu196Ala
|
|
|
ENST00000429182.5:c.381A>C
|
|
|
|
ENST00000442157.1:c.512A>C
|
ENSP00000403502.1:p.Glu171Ala
|
|
|
ENST00000462980.1:n.489A>C
|
|
|
|
ENST00000491610.1:n.474A>C
|
|
|
|
NM_000884.2:c.587A>C
|
NP_000875.2:p.Glu196Ala
|
|
|
XM_006713128.2:c.797A>C
|
XP_006713191.1:p.Glu266Ala
|
|
|
XM_006713128.3:c.797A>C
|
XP_006713191.1:p.Glu266Ala
|
|
|
XM_017006349.1:c.722A>C
|
XP_016861838.1:p.Glu241Ala
|
|
|
XM_017006350.1:c.722A>C
|
XP_016861839.1:p.Glu241Ala
|
|
|
NM_000884.3:c.587A>C
MANE Select
|
NP_000875.2:p.Glu196Ala
|
|
