|
ENST00000344642.7:c.*2105C>A
(LDLRAD2)
MANE Select
|
ENSP00000340988.2:n.*2105C>A
|
|
|
ENST00000374695.8:c.12801G>T
(HSPG2)
MANE Select
|
ENSP00000363827.3:p.Gly4267=
|
|
|
ENST00000344642.6:c.*2105C>A
(LDLRAD2)
|
ENSP00000340988.2:n.*2105C>A
|
|
|
ENST00000374695.7:c.12801G>T
(HSPG2)
|
ENSP00000363827.3:p.Gly4267=
|
|
|
ENST00000486901.1:n.2140G>T
(HSPG2)
|
|
|
|
NM_001013693.2:c.*2105C>A
(LDLRAD2)
|
NP_001013715.2:n.*2105C>A
|
|
|
NM_001291860.1:c.12804G>T
(HSPG2)
|
NP_001278789.1:p.Gly4268=
|
|
|
NM_005529.6:c.12801G>T
(HSPG2)
|
NP_005520.4:p.Gly4267=
|
|
|
XM_006710594.2:c.13365G>T
(HSPG2)
|
XP_006710657.1:p.Gly4455=
|
|
|
XM_006710595.2:c.13317G>T
(HSPG2)
|
XP_006710658.1:p.Gly4439=
|
|
|
XM_006710596.2:c.13296G>T
(HSPG2)
|
XP_006710659.1:p.Gly4432=
|
|
|
XM_006710597.2:c.12819G>T
(HSPG2)
|
XP_006710660.1:p.Gly4273=
|
|
|
XM_011541317.1:c.13368G>T
(HSPG2)
|
XP_011539619.1:p.Gly4456=
|
|
|
XM_011541318.1:c.13350G>T
(HSPG2)
|
XP_011539620.1:p.Gly4450=
|
|
|
XM_011541319.1:c.13245G>T
(HSPG2)
|
XP_011539621.1:p.Gly4415=
|
|
|
XM_011541320.1:c.13089G>T
(HSPG2)
|
XP_011539622.1:p.Gly4363=
|
|
|
XM_011541321.1:c.12873G>T
(HSPG2)
|
XP_011539623.1:p.Gly4291=
|
|
|
XM_011541318.2:c.13350G>T
(HSPG2)
|
XP_011539620.1:p.Gly4450=
|
|
|
XM_017001120.1:c.12996G>T
(HSPG2)
|
XP_016856609.1:p.Gly4332=
|
|
|
XM_017001121.1:c.12945G>T
(HSPG2)
|
XP_016856610.1:p.Gly4315=
|
|
|
XM_017001122.1:c.12942G>T
(HSPG2)
|
XP_016856611.1:p.Gly4314=
|
|
|
NM_005529.7:c.12801G>T
(HSPG2)
MANE Select
|
NP_005520.4:p.Gly4267=
|
|
|
NM_001013693.3:c.*2105C>A
(LDLRAD2)
MANE Select
|
NP_001013715.2:n.*2105C>A
|
|
|
NM_001291860.2:c.12804G>T
(HSPG2)
|
NP_001278789.1:p.Gly4268=
|
|
