|
ENST00000292535.12:c.3781C>T
MANE Select
|
ENSP00000292535.7:p.Arg1261Ter
|
|
|
ENST00000292538.9:c.1256-33888C>T
|
ENSP00000292538.4:n.1256-33888C>T
|
|
|
ENST00000437600.9:c.1250-33888C>T
|
ENSP00000414091.5:n.1250-33888C>T
|
|
|
ENST00000546411.7:c.3781C>T
|
ENSP00000450125.3:p.Arg1261Ter
|
|
|
ENST00000622516.6:c.1256-33888C>T
MANE Plus Clinical
|
ENSP00000484760.2:n.1256-33888C>T
|
|
|
ENST00000645010.1:c.3646C>T
|
ENSP00000496653.1:p.Arg1216Ter
|
|
|
ENST00000646649.1:c.3340C>T
|
ENSP00000494610.1:p.Arg1114Ter
|
|
|
ENST00000292535.11:c.3781C>T
|
ENSP00000292535.7:p.Arg1261Ter
|
|
|
ENST00000292538.8:c.1256-33888C>T
|
ENSP00000292538.4:n.1256-33888C>T
|
|
|
ENST00000360264.7:c.3814C>T
|
ENSP00000353401.3:p.Arg1272Ter
|
|
|
ENST00000393824.7:c.1139-33888C>T
|
ENSP00000377410.3:n.1139-33888C>T
|
|
|
ENST00000425244.6:c.1118-33888C>T
|
ENSP00000409745.2:n.1118-33888C>T
|
|
|
ENST00000437600.8:c.1256-33888C>T
|
ENSP00000414091.4:n.1256-33888C>T
|
|
|
ENST00000546411.6:c.3475C>T
|
ENSP00000450125.2:p.Arg1159Ter
|
|
|
ENST00000547394.6:c.1208-33888C>T
|
ENSP00000449371.2:n.1208-33888C>T
|
|
|
ENST00000549414.6:c.3715C>T
|
ENSP00000446630.2:p.Arg1239Ter
|
|
|
ENST00000550008.6:c.3613C>T
|
ENSP00000447373.2:p.Arg1205Ter
|
|
|
ENST00000556210.1:c.3307C>T
|
ENSP00000451558.1:p.Arg1103Ter
|
|
|
ENST00000558836.5:n.1362-33888C>T
|
|
|
|
ENST00000560541.5:n.1528-33888C>T
|
|
|
|
ENST00000622516.4:c.1250-33888C>T
|
ENSP00000484760.1:n.1250-33888C>T
|
|
|
NM_001202543.1:c.3814C>T
|
NP_001189472.1:p.Arg1272Ter
|
|
|
NM_001202544.2:c.1208-33888C>T
|
NP_001189473.1:n.1208-33888C>T
|
|
|
NM_001202545.2:c.1118-33888C>T
|
NP_001189474.1:n.1118-33888C>T
|
|
|
NM_001202546.2:c.1139-33888C>T
|
NP_001189475.1:n.1139-33888C>T
|
|
|
NM_001913.4:c.1256-33888C>T
|
NP_001904.2:n.1256-33888C>T
|
|
|
NM_181500.3:c.1250-33888C>T
|
NP_852477.1:n.1250-33888C>T
|
|
|
NM_181552.3:c.3781C>T
|
NP_853530.2:p.Arg1261Ter
|
|
|
XM_005250150.1:c.4078C>T
|
XP_005250207.1:p.Arg1360Ter
|
|
|
XM_005250151.1:c.4075C>T
|
XP_005250208.1:p.Arg1359Ter
|
|
|
XM_005250154.3:c.1523-33888C>T
|
XP_005250211.1:n.1523-33888C>T
|
|
|
XM_006715854.1:c.4015C>T
|
XP_006715917.1:p.Arg1339Ter
|
|
|
XM_006715855.1:c.1517-33888C>T
|
XP_006715918.1:n.1517-33888C>T
|
|
|
XM_006715856.2:c.3748C>T
|
XP_006715919.1:p.Arg1250Ter
|
|
|
XM_011515823.1:c.3775C>T
|
XP_011514125.1:p.Arg1259Ter
|
|
|
XM_011515824.1:c.3769C>T
|
XP_011514126.1:p.Arg1257Ter
|
|
|
XM_011515825.1:c.3508C>T
|
XP_011514127.1:p.Arg1170Ter
|
|
|
XM_005250150.3:c.4078C>T
|
XP_005250207.1:p.Arg1360Ter
|
|
|
XM_006715854.2:c.4015C>T
|
XP_006715917.1:p.Arg1339Ter
|
|
|
XM_011515825.2:c.3508C>T
|
XP_011514127.1:p.Arg1170Ter
|
|
|
XM_017011760.2:c.3742C>T
|
XP_016867249.1:p.Arg1248Ter
|
|
|
XM_024446668.1:c.3769C>T
|
XP_024302436.1:p.Arg1257Ter
|
|
|
NM_181552.4:c.3781C>T
MANE Select
|
NP_853530.2:p.Arg1261Ter
|
|
|
NM_001202543.2:c.3814C>T
|
NP_001189472.1:p.Arg1272Ter
|
|
|
NM_001202544.3:c.1208-33888C>T
|
NP_001189473.1:n.1208-33888C>T
|
|
|
NM_001202545.3:c.1118-33888C>T
|
NP_001189474.1:n.1118-33888C>T
|
|
|
NM_001202546.3:c.1139-33888C>T
|
NP_001189475.1:n.1139-33888C>T
|
|
|
NM_001913.5:c.1256-33888C>T
MANE Plus Clinical
|
NP_001904.2:n.1256-33888C>T
|
|
|
NM_181500.4:c.1250-33888C>T
|
NP_852477.1:n.1250-33888C>T
|
|
