|
ENST00000711048.1:c.1009-1687C>G
|
ENSP00000518557.1:n.1009-1687C>G
|
|
|
ENST00000402731.6:c.866C>G
|
ENSP00000384835.2:p.Ser289Ter
|
|
|
ENST00000404276.6:c.1067C>G
MANE Select
|
ENSP00000385747.1:p.Ser356Ter
|
|
|
ENST00000425190.7:c.404C>G
|
ENSP00000390244.2:p.Ser135Ter
|
|
|
ENST00000464581.6:c.407C>G
|
ENSP00000483777.2:p.Ser136Ter
|
|
|
ENST00000648295.1:n.619C>G
|
|
|
|
ENST00000649563.1:c.404C>G
|
ENSP00000496928.1:p.Ser135Ter
|
|
|
ENST00000650281.1:c.1067C>G
|
ENSP00000497000.1:p.Ser356Ter
|
|
|
ENST00000328354.10:c.1067C>G
|
ENSP00000329178.6:p.Ser356Ter
|
|
|
ENST00000348295.7:c.1009-1056C>G
|
ENSP00000329012.5:n.1009-1056C>G
|
|
|
ENST00000382580.6:c.1196C>G
|
ENSP00000372023.2:p.Ser399Ter
|
|
|
ENST00000402731.5:c.1009-1056C>G
|
ENSP00000384835.1:n.1009-1056C>G
|
|
|
ENST00000403642.5:c.794C>G
|
ENSP00000384919.1:p.Ser265Ter
|
|
|
ENST00000404276.5:c.1067C>G
|
ENSP00000385747.1:p.Ser356Ter
|
|
|
ENST00000405598.5:c.1067C>G
|
ENSP00000386087.1:p.Ser356Ter
|
|
|
ENST00000416671.5:c.*557C>G
|
ENSP00000402225.1:n.*557C>G
|
|
|
ENST00000417588.5:c.976C>G
|
ENSP00000412901.1:n.976C>G
|
|
|
ENST00000433028.6:c.*792C>G
|
ENSP00000403659.1:n.*792C>G
|
|
|
ENST00000433728.5:c.1005C>G
|
ENSP00000404400.1:n.1005C>G
|
|
|
ENST00000434810.5:c.298C>G
|
|
|
|
ENST00000447421.5:c.866C>G
|
ENSP00000397478.2:p.Ser289Ter
|
|
|
ENST00000448511.5:c.957C>G
|
ENSP00000404567.1:n.957C>G
|
|
|
ENST00000456369.5:c.263+2909C>G
|
|
|
|
ENST00000464581.5:c.407C>G
|
ENSP00000483777.1:p.Ser136Ter
|
|
|
NM_001005735.1:c.1196C>G
|
NP_001005735.1:p.Ser399Ter
|
|
|
NM_001257387.1:c.404C>G
|
NP_001244316.1:p.Ser135Ter
|
|
|
NM_007194.3:c.1067C>G
|
NP_009125.1:p.Ser356Ter
|
|
|
NM_145862.2:c.1009-1056C>G
|
NP_665861.1:n.1009-1056C>G
|
|
|
XM_006724114.2:c.587C>G
|
XP_006724177.1:p.Ser196Ter
|
|
|
XM_006724116.2:c.524C>G
|
XP_006724179.2:p.Ser175Ter
|
|
|
XM_011529839.1:c.1226C>G
|
XP_011528141.1:p.Ser409Ter
|
|
|
XM_011529840.1:c.1168-1056C>G
|
XP_011528142.1:n.1168-1056C>G
|
|
|
XM_011529841.1:c.995C>G
|
XP_011528143.1:p.Ser332Ter
|
|
|
XM_011529842.1:c.896C>G
|
XP_011528144.1:p.Ser299Ter
|
|
|
XM_011529843.1:c.866C>G
|
XP_011528145.1:p.Ser289Ter
|
|
|
XM_011529845.1:c.404C>G
|
XP_011528147.1:p.Ser135Ter
|
|
|
XR_937805.1:n.1226C>G
|
|
|
|
XR_937806.1:n.1163-1056C>G
|
|
|
|
NM_001349956.1:c.866C>G
|
NP_001336885.1:p.Ser289Ter
|
|
|
NM_007194.4:c.1067C>G
MANE Select
|
NP_009125.1:p.Ser356Ter
|
|
|
XM_006724114.3:c.620C>G
|
XP_006724177.2:p.Ser207Ter
|
|
|
XM_011529839.2:c.1226C>G
|
XP_011528141.1:p.Ser409Ter
|
|
|
XM_011529840.3:c.1168-1056C>G
|
XP_011528142.1:n.1168-1056C>G
|
|
|
XM_011529842.2:c.896C>G
|
XP_011528144.1:p.Ser299Ter
|
|
|
XM_011529845.2:c.404C>G
|
XP_011528147.1:p.Ser135Ter
|
|
|
XM_017028560.1:c.1190C>G
|
XP_016884049.1:p.Ser397Ter
|
|
|
XM_017028561.2:c.404C>G
|
XP_016884050.1:p.Ser135Ter
|
|
|
XM_024452148.1:c.1097C>G
|
XP_024307916.1:p.Ser366Ter
|
|
|
XM_024452149.1:c.1039-1056C>G
|
XP_024307917.1:n.1039-1056C>G
|
|
|
XR_937805.2:n.1237C>G
|
|
|
|
XR_937806.2:n.1179-1056C>G
|
|
|
|
NM_001005735.2:c.1196C>G
|
NP_001005735.1:p.Ser399Ter
|
|
|
NM_001257387.2:c.404C>G
|
NP_001244316.1:p.Ser135Ter
|
|
|
NM_001349956.2:c.866C>G
|
NP_001336885.1:p.Ser289Ter
|
|
