|
ENST00000703936.1:c.2847T>A
|
ENSP00000515567.1:p.Asp949Glu
|
|
|
ENST00000703937.1:c.*1908T>A
|
ENSP00000515568.1:n.*1908T>A
|
|
|
ENST00000326739.9:c.807T>A
MANE Select
|
ENSP00000321584.4:p.Asp269Glu
|
|
|
ENST00000429182.6:c.807T>A
|
ENSP00000393525.2:p.Asp269Glu
|
|
|
ENST00000442157.2:c.732T>A
|
ENSP00000403502.2:p.Asp244Glu
|
|
|
ENST00000462980.2:n.1322T>A
|
|
|
|
ENST00000472328.2:n.873T>A
|
|
|
|
ENST00000491610.2:n.767T>A
|
|
|
|
ENST00000676607.1:n.1103T>A
|
|
|
|
ENST00000676627.1:n.1537T>A
|
|
|
|
ENST00000676708.1:n.2087T>A
|
|
|
|
ENST00000676864.1:n.1956T>A
|
|
|
|
ENST00000677010.1:c.843T>A
|
ENSP00000503089.1:p.Asp281Glu
|
|
|
ENST00000677108.1:n.2713T>A
|
|
|
|
ENST00000677168.1:n.1279T>A
|
|
|
|
ENST00000677185.1:n.1370T>A
|
|
|
|
ENST00000677205.1:n.1591T>A
|
|
|
|
ENST00000677344.1:n.2081T>A
|
|
|
|
ENST00000677480.1:c.*484T>A
|
ENSP00000504378.1:n.*484T>A
|
|
|
ENST00000677519.1:n.1517T>A
|
|
|
|
ENST00000677593.1:n.1363T>A
|
|
|
|
ENST00000677740.1:n.2312T>A
|
|
|
|
ENST00000677991.1:n.1980T>A
|
|
|
|
ENST00000678001.1:n.1300T>A
|
|
|
|
ENST00000678085.1:n.1363T>A
|
|
|
|
ENST00000678177.1:n.2656T>A
|
|
|
|
ENST00000678603.1:n.1885T>A
|
|
|
|
ENST00000678724.1:c.732T>A
|
ENSP00000503874.1:p.Asp244Glu
|
|
|
ENST00000678920.1:n.965T>A
|
|
|
|
ENST00000679019.1:n.1577T>A
|
|
|
|
ENST00000679117.1:c.*622T>A
|
ENSP00000503240.1:n.*622T>A
|
|
|
ENST00000679339.1:n.1648T>A
|
|
|
|
ENST00000326739.8:c.807T>A
|
ENSP00000321584.4:p.Asp269Glu
|
|
|
ENST00000429182.5:c.601T>A
|
|
|
|
ENST00000442157.1:c.732T>A
|
ENSP00000403502.1:p.Asp244Glu
|
|
|
ENST00000462980.1:n.709T>A
|
|
|
|
ENST00000491610.1:n.767T>A
|
|
|
|
NM_000884.2:c.807T>A
|
NP_000875.2:p.Asp269Glu
|
|
|
XM_006713128.2:c.1017T>A
|
XP_006713191.1:p.Asp339Glu
|
|
|
XM_006713128.3:c.1017T>A
|
XP_006713191.1:p.Asp339Glu
|
|
|
XM_017006349.1:c.942T>A
|
XP_016861838.1:p.Asp314Glu
|
|
|
XM_017006350.1:c.942T>A
|
XP_016861839.1:p.Asp314Glu
|
|
|
NM_000884.3:c.807T>A
MANE Select
|
NP_000875.2:p.Asp269Glu
|
|
