ENST00000703936.1:c.2822A>T
|
ENSP00000515567.1:p.Asp941Val
|
|
ENST00000703937.1:c.*1883A>T
|
ENSP00000515568.1:n.*1883A>T
|
|
ENST00000326739.9:c.782A>T
MANE Select
|
ENSP00000321584.4:p.Asp261Val
|
|
ENST00000429182.6:c.782A>T
|
ENSP00000393525.2:p.Asp261Val
|
|
ENST00000442157.2:c.707A>T
|
ENSP00000403502.2:p.Asp236Val
|
|
ENST00000462980.2:n.1297A>T
|
|
|
ENST00000472328.2:n.848A>T
|
|
|
ENST00000491610.2:n.742A>T
|
|
|
ENST00000676607.1:n.1078A>T
|
|
|
ENST00000676627.1:n.1512A>T
|
|
|
ENST00000676708.1:n.2062A>T
|
|
|
ENST00000676864.1:n.1931A>T
|
|
|
ENST00000677010.1:c.818A>T
|
ENSP00000503089.1:p.Asp273Val
|
|
ENST00000677108.1:n.2688A>T
|
|
|
ENST00000677168.1:n.1254A>T
|
|
|
ENST00000677185.1:n.1345A>T
|
|
|
ENST00000677205.1:n.1566A>T
|
|
|
ENST00000677344.1:n.2056A>T
|
|
|
ENST00000677480.1:c.*459A>T
|
ENSP00000504378.1:n.*459A>T
|
|
ENST00000677519.1:n.1492A>T
|
|
|
ENST00000677593.1:n.1338A>T
|
|
|
ENST00000677740.1:n.2287A>T
|
|
|
ENST00000677991.1:n.1955A>T
|
|
|
ENST00000678001.1:n.1275A>T
|
|
|
ENST00000678085.1:n.1338A>T
|
|
|
ENST00000678177.1:n.2631A>T
|
|
|
ENST00000678603.1:n.1860A>T
|
|
|
ENST00000678724.1:c.707A>T
|
ENSP00000503874.1:p.Asp236Val
|
|
ENST00000678920.1:n.940A>T
|
|
|
ENST00000679019.1:n.1552A>T
|
|
|
ENST00000679117.1:c.*597A>T
|
ENSP00000503240.1:n.*597A>T
|
|
ENST00000679339.1:n.1623A>T
|
|
|
ENST00000326739.8:c.782A>T
|
ENSP00000321584.4:p.Asp261Val
|
|
ENST00000429182.5:c.576A>T
|
|
|
ENST00000442157.1:c.707A>T
|
ENSP00000403502.1:p.Asp236Val
|
|
ENST00000462980.1:n.684A>T
|
|
|
ENST00000491610.1:n.742A>T
|
|
|
NM_000884.2:c.782A>T
|
NP_000875.2:p.Asp261Val
|
|
XM_006713128.2:c.992A>T
|
XP_006713191.1:p.Asp331Val
|
|
XM_006713128.3:c.992A>T
|
XP_006713191.1:p.Asp331Val
|
|
XM_017006349.1:c.917A>T
|
XP_016861838.1:p.Asp306Val
|
|
XM_017006350.1:c.917A>T
|
XP_016861839.1:p.Asp306Val
|
|
NM_000884.3:c.782A>T
MANE Select
|
NP_000875.2:p.Asp261Val
|
|