|
ENST00000703936.1:c.2660G>T
|
ENSP00000515567.1:p.Gly887Val
|
|
|
ENST00000703937.1:c.*1721G>T
|
ENSP00000515568.1:n.*1721G>T
|
|
|
ENST00000326739.9:c.620G>T
MANE Select
|
ENSP00000321584.4:p.Gly207Val
|
|
|
ENST00000429182.6:c.620G>T
|
ENSP00000393525.2:p.Gly207Val
|
|
|
ENST00000442157.2:c.545G>T
|
ENSP00000403502.2:p.Gly182Val
|
|
|
ENST00000462980.2:n.1135G>T
|
|
|
|
ENST00000472328.2:n.686G>T
|
|
|
|
ENST00000491610.2:n.580G>T
|
|
|
|
ENST00000676607.1:n.916G>T
|
|
|
|
ENST00000676627.1:n.1350G>T
|
|
|
|
ENST00000676708.1:n.1900G>T
|
|
|
|
ENST00000676864.1:n.1769G>T
|
|
|
|
ENST00000677010.1:c.656G>T
|
ENSP00000503089.1:p.Gly219Val
|
|
|
ENST00000677108.1:n.2526G>T
|
|
|
|
ENST00000677168.1:n.1092G>T
|
|
|
|
ENST00000677185.1:n.1183G>T
|
|
|
|
ENST00000677205.1:n.1404G>T
|
|
|
|
ENST00000677344.1:n.1894G>T
|
|
|
|
ENST00000677480.1:c.*297G>T
|
ENSP00000504378.1:n.*297G>T
|
|
|
ENST00000677519.1:n.1330G>T
|
|
|
|
ENST00000677593.1:n.1176G>T
|
|
|
|
ENST00000677740.1:n.2125G>T
|
|
|
|
ENST00000677991.1:n.1793G>T
|
|
|
|
ENST00000678001.1:n.1113G>T
|
|
|
|
ENST00000678085.1:n.1176G>T
|
|
|
|
ENST00000678177.1:n.2469G>T
|
|
|
|
ENST00000678603.1:n.1698G>T
|
|
|
|
ENST00000678724.1:c.545G>T
|
ENSP00000503874.1:p.Gly182Val
|
|
|
ENST00000678920.1:n.778G>T
|
|
|
|
ENST00000679019.1:n.1390G>T
|
|
|
|
ENST00000679117.1:c.*435G>T
|
ENSP00000503240.1:n.*435G>T
|
|
|
ENST00000679339.1:n.1461G>T
|
|
|
|
ENST00000326739.8:c.620G>T
|
ENSP00000321584.4:p.Gly207Val
|
|
|
ENST00000429182.5:c.414G>T
|
|
|
|
ENST00000442157.1:c.545G>T
|
ENSP00000403502.1:p.Gly182Val
|
|
|
ENST00000462980.1:n.522G>T
|
|
|
|
ENST00000491610.1:n.580G>T
|
|
|
|
NM_000884.2:c.620G>T
|
NP_000875.2:p.Gly207Val
|
|
|
XM_006713128.2:c.830G>T
|
XP_006713191.1:p.Gly277Val
|
|
|
XM_006713128.3:c.830G>T
|
XP_006713191.1:p.Gly277Val
|
|
|
XM_017006349.1:c.755G>T
|
XP_016861838.1:p.Gly252Val
|
|
|
XM_017006350.1:c.755G>T
|
XP_016861839.1:p.Gly252Val
|
|
|
NM_000884.3:c.620G>T
MANE Select
|
NP_000875.2:p.Gly207Val
|
|
