|
ENST00000344642.7:c.*1244C>G
(LDLRAD2)
MANE Select
|
ENSP00000340988.2:n.*1244C>G
|
|
|
ENST00000374695.8:c.13033G>C
(HSPG2)
MANE Select
|
ENSP00000363827.3:p.Gly4345Arg
|
|
|
ENST00000344642.6:c.*1244C>G
(LDLRAD2)
|
ENSP00000340988.2:n.*1244C>G
|
|
|
ENST00000374695.7:c.13033G>C
(HSPG2)
|
ENSP00000363827.3:p.Gly4345Arg
|
|
|
ENST00000481644.1:n.681G>C
(HSPG2)
|
|
|
|
ENST00000486901.1:n.2372G>C
(HSPG2)
|
|
|
|
ENST00000543870.1:c.*219-451C>G
(LDLRAD2)
|
ENSP00000444097.1:n.*219-451C>G
|
|
|
NM_001013693.2:c.*1244C>G
(LDLRAD2)
|
NP_001013715.2:n.*1244C>G
|
|
|
NM_001291860.1:c.13036G>C
(HSPG2)
|
NP_001278789.1:p.Gly4346Arg
|
|
|
NM_005529.6:c.13033G>C
(HSPG2)
|
NP_005520.4:p.Gly4345Arg
|
|
|
XM_006710594.2:c.13597G>C
(HSPG2)
|
XP_006710657.1:p.Gly4533Arg
|
|
|
XM_006710595.2:c.13549G>C
(HSPG2)
|
XP_006710658.1:p.Gly4517Arg
|
|
|
XM_006710596.2:c.13528G>C
(HSPG2)
|
XP_006710659.1:p.Gly4510Arg
|
|
|
XM_006710597.2:c.13051G>C
(HSPG2)
|
XP_006710660.1:p.Gly4351Arg
|
|
|
XM_011541317.1:c.13600G>C
(HSPG2)
|
XP_011539619.1:p.Gly4534Arg
|
|
|
XM_011541318.1:c.13582G>C
(HSPG2)
|
XP_011539620.1:p.Gly4528Arg
|
|
|
XM_011541319.1:c.13477G>C
(HSPG2)
|
XP_011539621.1:p.Gly4493Arg
|
|
|
XM_011541320.1:c.13321G>C
(HSPG2)
|
XP_011539622.1:p.Gly4441Arg
|
|
|
XM_011541321.1:c.13105G>C
(HSPG2)
|
XP_011539623.1:p.Gly4369Arg
|
|
|
XM_011541318.2:c.13582G>C
(HSPG2)
|
XP_011539620.1:p.Gly4528Arg
|
|
|
XM_017001120.1:c.13228G>C
(HSPG2)
|
XP_016856609.1:p.Gly4410Arg
|
|
|
XM_017001121.1:c.13177G>C
(HSPG2)
|
XP_016856610.1:p.Gly4393Arg
|
|
|
XM_017001122.1:c.13174G>C
(HSPG2)
|
XP_016856611.1:p.Gly4392Arg
|
|
|
NM_005529.7:c.13033G>C
(HSPG2)
MANE Select
|
NP_005520.4:p.Gly4345Arg
|
|
|
NM_001013693.3:c.*1244C>G
(LDLRAD2)
MANE Select
|
NP_001013715.2:n.*1244C>G
|
|
|
NM_001291860.2:c.13036G>C
(HSPG2)
|
NP_001278789.1:p.Gly4346Arg
|
|
