ENST00000411732.4:c.549G>C
|
ENSP00000387634.1:p.Gln183His
|
|
ENST00000439032.6:c.1239G>C
|
ENSP00000509775.1:n.1239G>C
|
|
ENST00000637191.2:c.699G>C
|
ENSP00000490154.2:p.Gln233His
|
|
ENST00000690143.1:c.*631G>C
|
ENSP00000510306.1:n.*631G>C
|
|
ENST00000691610.1:c.738G>C
|
ENSP00000509830.1:p.Gln246His
|
|
ENST00000242480.4:c.699G>C
MANE Select
|
ENSP00000242480.3:p.Gln233His
|
|
ENST00000411732.3:c.549G>C
|
ENSP00000387634.1:p.Gln183His
|
|
ENST00000639815.1:n.109-977G>C
|
|
|
ENST00000242480.3:c.699G>C
|
ENSP00000242480.3:p.Gln233His
|
|
ENST00000411732.2:c.549G>C
|
ENSP00000387634.1:p.Gln183His
|
|
ENST00000439032.4:c.699G>C
|
ENSP00000402040.1:p.Gln233His
|
|
NM_000399.3:c.699G>C , LRG_239t1:c.699G>C
|
NP_000390.2:p.Gln233His
|
|
NM_001136177.1:c.699G>C
|
NP_001129649.1:p.Gln233His
|
|
NM_001136178.1:c.699G>C
|
NP_001129650.1:p.Gln233His
|
|
NM_001136179.1:c.549G>C
|
NP_001129651.1:p.Gln183His
|
|
XM_011539427.1:c.738G>C
|
XP_011537729.1:p.Gln246His
|
|
XM_011539428.1:c.549G>C
|
XP_011537730.1:p.Gln183His
|
|
XM_011539429.1:c.549G>C
|
XP_011537731.1:p.Gln183His
|
|
NM_000399.4:c.699G>C
|
NP_000390.2:p.Gln233His
|
|
NM_001136177.2:c.699G>C
|
NP_001129649.1:p.Gln233His
|
|
NM_001136179.2:c.549G>C
|
NP_001129651.1:p.Gln183His
|
|
NM_001321037.1:c.549G>C
|
NP_001307966.1:p.Gln183His
|
|
NM_000399.5:c.699G>C
MANE Select
|
NP_000390.2:p.Gln233His
|
|
NM_001136177.3:c.699G>C
|
NP_001129649.1:p.Gln233His
|
|
NM_001136179.3:c.549G>C
|
NP_001129651.1:p.Gln183His
|
|
NM_001321037.2:c.549G>C
|
NP_001307966.1:p.Gln183His
|
|
NM_001136178.2:c.699G>C
|
NP_001129650.1:p.Gln233His
|
|