ENST00000700148.1:n.1583G>C
|
|
|
ENST00000700151.1:n.3849G>C
|
|
|
ENST00000700152.1:n.3389G>C
|
|
|
ENST00000700153.1:n.2763G>C
|
|
|
ENST00000700154.1:n.927G>C
|
|
|
ENST00000357234.10:c.1347G>C
MANE Select
|
ENSP00000349770.5:p.Glu449Asp
|
|
ENST00000489702.6:c.1347G>C
|
ENSP00000418037.2:p.Glu449Asp
|
|
ENST00000249375.8:c.1299G>C
|
ENSP00000249375.4:p.Glu433Asp
|
|
ENST00000357234.9:c.1347G>C
|
ENSP00000349770.5:p.Glu449Asp
|
|
ENST00000402030.6:c.1299G>C
|
ENSP00000385352.2:p.Glu433Asp
|
|
ENST00000465603.5:c.*827G>C
|
ENSP00000418534.1:n.*827G>C
|
|
ENST00000473745.5:c.1299G>C
|
ENSP00000419149.1:p.Glu433Asp
|
|
ENST00000477535.5:c.1041G>C
|
ENSP00000419950.1:p.Glu347Asp
|
|
ENST00000619830.1:c.*797G>C
|
ENSP00000483292.1:n.*797G>C
|
|
NM_001098627.3:c.1299G>C
|
NP_001092097.2:p.Glu433Asp
|
|
NM_001098629.2:c.1347G>C
|
NP_001092099.1:p.Glu449Asp
|
|
NM_001098630.2:c.1299G>C
|
NP_001092100.1:p.Glu433Asp
|
|
NM_001242452.2:c.1041G>C
|
NP_001229381.1:p.Glu347Asp
|
|
NM_032643.4:c.1299G>C
|
NP_116032.1:p.Glu433Asp
|
|
XM_005250317.2:c.1347G>C
|
XP_005250374.1:p.Glu449Asp
|
|
XM_006715974.2:c.1347G>C
|
XP_006716037.1:p.Glu449Asp
|
|
XM_011516158.1:c.1347G>C
|
XP_011514460.1:p.Glu449Asp
|
|
XM_011516159.1:c.1347G>C
|
XP_011514461.1:p.Glu449Asp
|
|
XM_011516160.1:c.1347G>C
|
XP_011514462.1:p.Glu449Asp
|
|
XM_011516161.1:c.1317G>C
|
XP_011514463.1:p.Glu439Asp
|
|
XM_011516162.1:c.1269G>C
|
XP_011514464.1:p.Glu423Asp
|
|
XM_011516163.1:c.1269G>C
|
XP_011514465.1:p.Glu423Asp
|
|
XM_011516164.1:c.1269G>C
|
XP_011514466.1:p.Glu423Asp
|
|
NM_001347928.1:c.1347G>C
|
NP_001334857.1:p.Glu449Asp
|
|
NM_001364314.1:c.1347G>C
|
NP_001351243.1:p.Glu449Asp
|
|
XM_011516158.3:c.1347G>C
|
XP_011514460.1:p.Glu449Asp
|
|
XM_011516159.3:c.1347G>C
|
XP_011514461.1:p.Glu449Asp
|
|
NM_001098629.3:c.1347G>C
MANE Select
|
NP_001092099.1:p.Glu449Asp
|
|
NM_001098630.3:c.1299G>C
|
NP_001092100.1:p.Glu433Asp
|
|
NM_001242452.3:c.1041G>C
|
NP_001229381.1:p.Glu347Asp
|
|
NM_001347928.2:c.1347G>C
|
NP_001334857.1:p.Glu449Asp
|
|
NM_001364314.2:c.1347G>C
|
NP_001351243.1:p.Glu449Asp
|
|
NM_001098627.4:c.1299G>C
|
NP_001092097.2:p.Glu433Asp
|
|
NM_032643.5:c.1299G>C
|
NP_116032.1:p.Glu433Asp
|
|