|
ENST00000703936.1:c.2690A>C
|
ENSP00000515567.1:p.Glu897Ala
|
|
|
ENST00000703937.1:c.*1751A>C
|
ENSP00000515568.1:n.*1751A>C
|
|
|
ENST00000326739.9:c.650A>C
MANE Select
|
ENSP00000321584.4:p.Glu217Ala
|
|
|
ENST00000429182.6:c.650A>C
|
ENSP00000393525.2:p.Glu217Ala
|
|
|
ENST00000442157.2:c.575A>C
|
ENSP00000403502.2:p.Glu192Ala
|
|
|
ENST00000462980.2:n.1165A>C
|
|
|
|
ENST00000472328.2:n.716A>C
|
|
|
|
ENST00000491610.2:n.610A>C
|
|
|
|
ENST00000676607.1:n.946A>C
|
|
|
|
ENST00000676627.1:n.1380A>C
|
|
|
|
ENST00000676708.1:n.1930A>C
|
|
|
|
ENST00000676864.1:n.1799A>C
|
|
|
|
ENST00000677010.1:c.686A>C
|
ENSP00000503089.1:p.Glu229Ala
|
|
|
ENST00000677108.1:n.2556A>C
|
|
|
|
ENST00000677168.1:n.1122A>C
|
|
|
|
ENST00000677185.1:n.1213A>C
|
|
|
|
ENST00000677205.1:n.1434A>C
|
|
|
|
ENST00000677344.1:n.1924A>C
|
|
|
|
ENST00000677480.1:c.*327A>C
|
ENSP00000504378.1:n.*327A>C
|
|
|
ENST00000677519.1:n.1360A>C
|
|
|
|
ENST00000677593.1:n.1206A>C
|
|
|
|
ENST00000677740.1:n.2155A>C
|
|
|
|
ENST00000677991.1:n.1823A>C
|
|
|
|
ENST00000678001.1:n.1143A>C
|
|
|
|
ENST00000678085.1:n.1206A>C
|
|
|
|
ENST00000678177.1:n.2499A>C
|
|
|
|
ENST00000678603.1:n.1728A>C
|
|
|
|
ENST00000678724.1:c.575A>C
|
ENSP00000503874.1:p.Glu192Ala
|
|
|
ENST00000678920.1:n.808A>C
|
|
|
|
ENST00000679019.1:n.1420A>C
|
|
|
|
ENST00000679117.1:c.*465A>C
|
ENSP00000503240.1:n.*465A>C
|
|
|
ENST00000679339.1:n.1491A>C
|
|
|
|
ENST00000326739.8:c.650A>C
|
ENSP00000321584.4:p.Glu217Ala
|
|
|
ENST00000429182.5:c.444A>C
|
|
|
|
ENST00000442157.1:c.575A>C
|
ENSP00000403502.1:p.Glu192Ala
|
|
|
ENST00000462980.1:n.552A>C
|
|
|
|
ENST00000491610.1:n.610A>C
|
|
|
|
NM_000884.2:c.650A>C
|
NP_000875.2:p.Glu217Ala
|
|
|
XM_006713128.2:c.860A>C
|
XP_006713191.1:p.Glu287Ala
|
|
|
XM_006713128.3:c.860A>C
|
XP_006713191.1:p.Glu287Ala
|
|
|
XM_017006349.1:c.785A>C
|
XP_016861838.1:p.Glu262Ala
|
|
|
XM_017006350.1:c.785A>C
|
XP_016861839.1:p.Glu262Ala
|
|
|
NM_000884.3:c.650A>C
MANE Select
|
NP_000875.2:p.Glu217Ala
|
|
