|
ENST00000703936.1:c.2687A>T
|
ENSP00000515567.1:p.Asp896Val
|
|
|
ENST00000703937.1:c.*1748A>T
|
ENSP00000515568.1:n.*1748A>T
|
|
|
ENST00000326739.9:c.647A>T
MANE Select
|
ENSP00000321584.4:p.Asp216Val
|
|
|
ENST00000429182.6:c.647A>T
|
ENSP00000393525.2:p.Asp216Val
|
|
|
ENST00000442157.2:c.572A>T
|
ENSP00000403502.2:p.Asp191Val
|
|
|
ENST00000462980.2:n.1162A>T
|
|
|
|
ENST00000472328.2:n.713A>T
|
|
|
|
ENST00000491610.2:n.607A>T
|
|
|
|
ENST00000676607.1:n.943A>T
|
|
|
|
ENST00000676627.1:n.1377A>T
|
|
|
|
ENST00000676708.1:n.1927A>T
|
|
|
|
ENST00000676864.1:n.1796A>T
|
|
|
|
ENST00000677010.1:c.683A>T
|
ENSP00000503089.1:p.Asp228Val
|
|
|
ENST00000677108.1:n.2553A>T
|
|
|
|
ENST00000677168.1:n.1119A>T
|
|
|
|
ENST00000677185.1:n.1210A>T
|
|
|
|
ENST00000677205.1:n.1431A>T
|
|
|
|
ENST00000677344.1:n.1921A>T
|
|
|
|
ENST00000677480.1:c.*324A>T
|
ENSP00000504378.1:n.*324A>T
|
|
|
ENST00000677519.1:n.1357A>T
|
|
|
|
ENST00000677593.1:n.1203A>T
|
|
|
|
ENST00000677740.1:n.2152A>T
|
|
|
|
ENST00000677991.1:n.1820A>T
|
|
|
|
ENST00000678001.1:n.1140A>T
|
|
|
|
ENST00000678085.1:n.1203A>T
|
|
|
|
ENST00000678177.1:n.2496A>T
|
|
|
|
ENST00000678603.1:n.1725A>T
|
|
|
|
ENST00000678724.1:c.572A>T
|
ENSP00000503874.1:p.Asp191Val
|
|
|
ENST00000678920.1:n.805A>T
|
|
|
|
ENST00000679019.1:n.1417A>T
|
|
|
|
ENST00000679117.1:c.*462A>T
|
ENSP00000503240.1:n.*462A>T
|
|
|
ENST00000679339.1:n.1488A>T
|
|
|
|
ENST00000326739.8:c.647A>T
|
ENSP00000321584.4:p.Asp216Val
|
|
|
ENST00000429182.5:c.441A>T
|
|
|
|
ENST00000442157.1:c.572A>T
|
ENSP00000403502.1:p.Asp191Val
|
|
|
ENST00000462980.1:n.549A>T
|
|
|
|
ENST00000491610.1:n.607A>T
|
|
|
|
NM_000884.2:c.647A>T
|
NP_000875.2:p.Asp216Val
|
|
|
XM_006713128.2:c.857A>T
|
XP_006713191.1:p.Asp286Val
|
|
|
XM_006713128.3:c.857A>T
|
XP_006713191.1:p.Asp286Val
|
|
|
XM_017006349.1:c.782A>T
|
XP_016861838.1:p.Asp261Val
|
|
|
XM_017006350.1:c.782A>T
|
XP_016861839.1:p.Asp261Val
|
|
|
NM_000884.3:c.647A>T
MANE Select
|
NP_000875.2:p.Asp216Val
|
|
