ENST00000561028.6:c.546G>C
MANE Select
|
ENSP00000454062.2:p.Gln182His
|
|
ENST00000396995.1:c.129G>C
|
ENSP00000380191.1:p.Gln43His
|
|
ENST00000396997.1:c.546G>C
|
ENSP00000380193.1:p.Gln182His
|
|
ENST00000397002.6:c.546G>C
|
ENSP00000380197.2:p.Gln182His
|
|
ENST00000560550.1:c.129G>C
|
ENSP00000452966.1:p.Gln43His
|
|
ENST00000561028.5:c.546G>C
|
ENSP00000454062.1:p.Gln182His
|
|
NM_006177.3:c.546G>C
|
NP_006168.1:p.Gln182His
|
|
XM_005267708.3:c.546G>C
|
XP_005267765.1:p.Gln182His
|
|
XM_005267709.3:c.546G>C
|
XP_005267766.1:p.Gln182His
|
|
XM_005267710.3:c.546G>C
|
XP_005267767.1:p.Gln182His
|
|
XM_011536801.1:c.645G>C
|
XP_011535103.1:p.Gln215His
|
|
XM_011536802.1:c.546G>C
|
XP_011535104.1:p.Gln182His
|
|
XM_011536803.1:c.546G>C
|
XP_011535105.1:p.Gln182His
|
|
XM_011536804.1:c.546G>C
|
XP_011535106.1:p.Gln182His
|
|
XM_011536805.1:c.546G>C
|
XP_011535107.1:p.Gln182His
|
|
XM_011536806.1:c.330G>C
|
XP_011535108.1:p.Gln110His
|
|
NM_001354768.1:c.546G>C
|
NP_001341697.1:p.Gln182His
|
|
NM_001354769.1:c.546G>C
|
NP_001341698.1:p.Gln182His
|
|
NM_001354770.1:c.231G>C
|
NP_001341699.1:p.Gln77His
|
|
NM_006177.4:c.546G>C
|
NP_006168.1:p.Gln182His
|
|
XM_011536801.2:c.852G>C
|
XP_011535103.2:p.Gln284His
|
|
XM_011536804.2:c.546G>C
|
XP_011535106.1:p.Gln182His
|
|
XM_011536805.2:c.546G>C
|
XP_011535107.1:p.Gln182His
|
|
XM_011536806.2:c.537G>C
|
XP_011535108.2:p.Gln179His
|
|
NM_001354768.3:c.546G>C
MANE Select
|
NP_001341697.1:p.Gln182His
|
|
NM_001354770.2:c.231G>C
|
NP_001341699.1:p.Gln77His
|
|
NM_006177.5:c.546G>C
|
NP_006168.1:p.Gln182His
|
|