ENST00000373207.2:c.3078G>T
MANE Select
|
ENSP00000362303.1:p.Gln1026His
|
|
ENST00000373207.1:c.3078G>T
|
ENSP00000362303.1:p.Gln1026His
|
|
ENST00000373208.5:c.3087G>T
|
ENSP00000362304.1:p.Gln1029His
|
|
NM_080722.3:c.3078G>T
|
NP_542453.2:p.Gln1026His
|
|
NM_139155.2:c.3087G>T
|
NP_631894.2:p.Gln1029His
|
|
XM_011539300.1:c.2577G>T
|
XP_011537602.1:p.Gln859His
|
|
XM_011539301.1:c.2151G>T
|
XP_011537603.1:p.Gln717His
|
|
XM_011539302.1:c.2151G>T
|
XP_011537604.1:p.Gln717His
|
|
XM_011539309.1:c.1647G>T
|
XP_011537611.1:p.Gln549His
|
|
NM_080722.4:c.3078G>T
MANE Select
|
NP_542453.2:p.Gln1026His
|
|
NM_139155.3:c.3087G>T
|
NP_631894.2:p.Gln1029His
|
|
XM_011539300.2:c.2577G>T
|
XP_011537602.1:p.Gln859His
|
|
XM_011539301.2:c.2151G>T
|
XP_011537603.1:p.Gln717His
|
|
XM_011539302.2:c.2151G>T
|
XP_011537604.1:p.Gln717His
|
|