ENST00000373207.2:c.2970G>C
MANE Select
|
ENSP00000362303.1:p.Gln990His
|
|
ENST00000373207.1:c.2970G>C
|
ENSP00000362303.1:p.Gln990His
|
|
ENST00000373208.5:c.2979G>C
|
ENSP00000362304.1:p.Gln993His
|
|
NM_080722.3:c.2970G>C
|
NP_542453.2:p.Gln990His
|
|
NM_139155.2:c.2979G>C
|
NP_631894.2:p.Gln993His
|
|
XM_011539300.1:c.2469G>C
|
XP_011537602.1:p.Gln823His
|
|
XM_011539301.1:c.2043G>C
|
XP_011537603.1:p.Gln681His
|
|
XM_011539302.1:c.2043G>C
|
XP_011537604.1:p.Gln681His
|
|
XM_011539308.1:c.*49G>C
|
XP_011537610.1:n.*49G>C
|
|
XM_011539309.1:c.1539G>C
|
XP_011537611.1:p.Gln513His
|
|
NM_080722.4:c.2970G>C
MANE Select
|
NP_542453.2:p.Gln990His
|
|
NM_139155.3:c.2979G>C
|
NP_631894.2:p.Gln993His
|
|
XM_011539300.2:c.2469G>C
|
XP_011537602.1:p.Gln823His
|
|
XM_011539301.2:c.2043G>C
|
XP_011537603.1:p.Gln681His
|
|
XM_011539302.2:c.2043G>C
|
XP_011537604.1:p.Gln681His
|
|
XM_011539308.2:c.*49G>C
|
XP_011537610.1:n.*49G>C
|
|