ENST00000474574.2:n.3081G>C
|
|
|
ENST00000487058.2:n.1253G>C
|
|
|
ENST00000681987.1:n.1344G>C
|
|
|
ENST00000681988.1:c.1005G>C
|
ENSP00000507316.1:p.Glu335Asp
|
|
ENST00000682396.1:c.1497G>C
|
ENSP00000506764.1:n.1497G>C
|
|
ENST00000682507.1:c.1005G>C
|
ENSP00000508098.1:p.Glu335Asp
|
|
ENST00000682622.1:c.1786G>C
|
ENSP00000506732.1:n.1786G>C
|
|
ENST00000682833.1:c.1341G>C
|
|
|
ENST00000683022.1:c.1527G>C
|
|
|
ENST00000683256.1:c.1005G>C
|
ENSP00000507901.1:p.Glu335Asp
|
|
ENST00000683269.1:c.1005G>C
|
ENSP00000508107.1:p.Glu335Asp
|
|
ENST00000683647.1:n.4840G>C
|
|
|
ENST00000683649.1:n.356G>C
|
|
|
ENST00000683783.1:c.1005G>C
|
ENSP00000507881.1:p.Glu335Asp
|
|
ENST00000683813.1:n.1234G>C
|
|
|
ENST00000684032.1:c.1361G>C
|
ENSP00000506969.1:n.1361G>C
|
|
ENST00000684201.1:c.1230G>C
|
ENSP00000507887.1:p.Glu410Asp
|
|
ENST00000684338.1:c.1506G>C
|
ENSP00000507457.1:p.Glu502Asp
|
|
ENST00000684372.1:c.1005G>C
|
ENSP00000508244.1:p.Glu335Asp
|
|
ENST00000684434.1:c.977G>C
|
|
|
ENST00000684546.1:c.1005G>C
|
ENSP00000507729.1:p.Glu335Asp
|
|
ENST00000684665.1:n.470G>C
|
|
|
ENST00000684690.1:n.1733G>C
|
|
|
ENST00000684699.1:n.4085G>C
|
|
|
ENST00000277865.5:c.1506G>C
MANE Select
|
ENSP00000277865.4:p.Glu502Asp
|
|
ENST00000277865.4:c.1506G>C
|
ENSP00000277865.4:p.Glu502Asp
|
|
NM_005271.3:c.1506G>C
|
NP_005262.1:p.Glu502Asp
|
|
XM_011539668.1:c.1005G>C
|
XP_011537970.1:p.Glu335Asp
|
|
XM_011539669.1:c.1005G>C
|
XP_011537971.1:p.Glu335Asp
|
|
NM_001318900.1:c.1107G>C
|
NP_001305829.1:p.Glu369Asp
|
|
NM_001318901.1:c.1005G>C
|
NP_001305830.1:p.Glu335Asp
|
|
NM_001318902.1:c.1005G>C
|
NP_001305831.1:p.Glu335Asp
|
|
NM_001318904.1:c.1005G>C
|
NP_001305833.1:p.Glu335Asp
|
|
NM_001318905.1:c.1005G>C
|
NP_001305834.1:p.Glu335Asp
|
|
NM_001318906.1:c.1005G>C
|
NP_001305835.1:p.Glu335Asp
|
|
NM_005271.4:c.1506G>C
|
NP_005262.1:p.Glu502Asp
|
|
NM_005271.5:c.1506G>C
MANE Select
|
NP_005262.1:p.Glu502Asp
|
|
NM_001318904.2:c.1005G>C
|
NP_001305833.1:p.Glu335Asp
|
|
NM_001318905.2:c.1005G>C
|
NP_001305834.1:p.Glu335Asp
|
|
NM_001318906.2:c.1005G>C
|
NP_001305835.1:p.Glu335Asp
|
|