|
ENST00000703936.1:c.2801A>T
|
ENSP00000515567.1:p.Glu934Val
|
|
|
ENST00000703937.1:c.*1862A>T
|
ENSP00000515568.1:n.*1862A>T
|
|
|
ENST00000326739.9:c.761A>T
MANE Select
|
ENSP00000321584.4:p.Glu254Val
|
|
|
ENST00000429182.6:c.761A>T
|
ENSP00000393525.2:p.Glu254Val
|
|
|
ENST00000442157.2:c.686A>T
|
ENSP00000403502.2:p.Glu229Val
|
|
|
ENST00000462980.2:n.1276A>T
|
|
|
|
ENST00000472328.2:n.827A>T
|
|
|
|
ENST00000491610.2:n.721A>T
|
|
|
|
ENST00000676607.1:n.1057A>T
|
|
|
|
ENST00000676627.1:n.1491A>T
|
|
|
|
ENST00000676708.1:n.2041A>T
|
|
|
|
ENST00000676864.1:n.1910A>T
|
|
|
|
ENST00000677010.1:c.797A>T
|
ENSP00000503089.1:p.Glu266Val
|
|
|
ENST00000677108.1:n.2667A>T
|
|
|
|
ENST00000677168.1:n.1233A>T
|
|
|
|
ENST00000677185.1:n.1324A>T
|
|
|
|
ENST00000677205.1:n.1545A>T
|
|
|
|
ENST00000677344.1:n.2035A>T
|
|
|
|
ENST00000677480.1:c.*438A>T
|
ENSP00000504378.1:n.*438A>T
|
|
|
ENST00000677519.1:n.1471A>T
|
|
|
|
ENST00000677593.1:n.1317A>T
|
|
|
|
ENST00000677740.1:n.2266A>T
|
|
|
|
ENST00000677991.1:n.1934A>T
|
|
|
|
ENST00000678001.1:n.1254A>T
|
|
|
|
ENST00000678085.1:n.1317A>T
|
|
|
|
ENST00000678177.1:n.2610A>T
|
|
|
|
ENST00000678603.1:n.1839A>T
|
|
|
|
ENST00000678724.1:c.686A>T
|
ENSP00000503874.1:p.Glu229Val
|
|
|
ENST00000678920.1:n.919A>T
|
|
|
|
ENST00000679019.1:n.1531A>T
|
|
|
|
ENST00000679117.1:c.*576A>T
|
ENSP00000503240.1:n.*576A>T
|
|
|
ENST00000679339.1:n.1602A>T
|
|
|
|
ENST00000326739.8:c.761A>T
|
ENSP00000321584.4:p.Glu254Val
|
|
|
ENST00000429182.5:c.555A>T
|
|
|
|
ENST00000442157.1:c.686A>T
|
ENSP00000403502.1:p.Glu229Val
|
|
|
ENST00000462980.1:n.663A>T
|
|
|
|
ENST00000491610.1:n.721A>T
|
|
|
|
NM_000884.2:c.761A>T
|
NP_000875.2:p.Glu254Val
|
|
|
XM_006713128.2:c.971A>T
|
XP_006713191.1:p.Glu324Val
|
|
|
XM_006713128.3:c.971A>T
|
XP_006713191.1:p.Glu324Val
|
|
|
XM_017006349.1:c.896A>T
|
XP_016861838.1:p.Glu299Val
|
|
|
XM_017006350.1:c.896A>T
|
XP_016861839.1:p.Glu299Val
|
|
|
NM_000884.3:c.761A>T
MANE Select
|
NP_000875.2:p.Glu254Val
|
|
