ENST00000316891.10:c.915G>C
MANE Select
|
ENSP00000321810.5:p.Gln305His
|
|
ENST00000648678.1:c.1807G>C
|
ENSP00000497805.1:n.1807G>C
|
|
ENST00000316891.9:c.915G>C
|
ENSP00000321810.5:p.Gln305His
|
|
ENST00000372818.5:c.915G>C
|
ENSP00000361905.1:p.Gln305His
|
|
ENST00000441669.6:c.669G>C
|
ENSP00000388333.2:p.Gln223His
|
|
ENST00000462797.5:c.915G>C
|
ENSP00000473773.1:p.Gln305His
|
|
ENST00000465417.5:n.113-264G>C
|
|
|
ENST00000467774.1:n.197G>C
|
|
|
ENST00000486825.6:c.820G>C
|
|
|
ENST00000489945.5:c.*333G>C
|
ENSP00000473745.1:n.*333G>C
|
|
ENST00000491865.5:n.164-264G>C
|
|
|
ENST00000492612.6:c.759G>C
|
|
|
ENST00000495175.6:c.*337G>C
|
ENSP00000474264.1:n.*337G>C
|
|
ENST00000537440.5:c.17-264G>C
|
ENSP00000437700.1:n.17-264G>C
|
|
ENST00000541099.5:c.-140-2921G>C
|
ENSP00000437896.1:n.-140-2921G>C
|
|
NM_001312691.1:c.915G>C
|
NP_001299620.1:p.Gln305His
|
|
NM_001312692.1:c.669G>C
|
NP_001299621.1:p.Gln223His
|
|
NM_017646.4:c.915G>C
|
NP_060116.2:p.Gln305His
|
|
NM_017646.5:c.915G>C
|
NP_060116.2:p.Gln305His
|
|
NR_132401.1:n.931G>C
|
|
|
NR_132402.1:n.789G>C
|
|
|
NR_132403.1:n.785G>C
|
|
|
NR_132404.1:n.785G>C
|
|
|
NR_132405.1:n.781G>C
|
|
|
NR_132406.1:n.686-264G>C
|
|
|
NR_132407.1:n.549G>C
|
|
|
NR_132408.1:n.545G>C
|
|
|
NR_132409.1:n.406G>C
|
|
|
NR_132410.1:n.446-264G>C
|
|
|
NR_132412.1:n.307-264G>C
|
|
|
NR_132413.1:n.195-2921G>C
|
|
|
NR_132414.1:n.195-5648G>C
|
|
|
NR_132415.1:n.1022G>C
|
|
|
XM_005270954.1:c.672G>C
|
XP_005271011.1:p.Gln224His
|
|
XM_006710706.1:c.492G>C
|
XP_006710769.1:p.Gln164His
|
|
XM_005270954.2:c.672G>C
|
XP_005271011.1:p.Gln224His
|
|
XR_946672.2:n.1015G>C
|
|
|
NM_017646.6:c.915G>C
MANE Select
|
NP_060116.2:p.Gln305His
|
|