|
ENST00000292535.12:c.3563G>A
MANE Select
|
ENSP00000292535.7:p.Trp1188Ter
|
|
|
ENST00000292538.9:c.1255+38578G>A
|
ENSP00000292538.4:n.1255+38578G>A
|
|
|
ENST00000437600.9:c.1249+38578G>A
|
ENSP00000414091.5:n.1249+38578G>A
|
|
|
ENST00000546411.7:c.3563G>A
|
ENSP00000450125.3:p.Trp1188Ter
|
|
|
ENST00000622516.6:c.1255+38578G>A
MANE Plus Clinical
|
ENSP00000484760.2:n.1255+38578G>A
|
|
|
ENST00000645010.1:c.3428G>A
|
ENSP00000496653.1:p.Trp1143Ter
|
|
|
ENST00000646649.1:c.3122G>A
|
ENSP00000494610.1:p.Trp1041Ter
|
|
|
ENST00000292535.11:c.3563G>A
|
ENSP00000292535.7:p.Trp1188Ter
|
|
|
ENST00000292538.8:c.1255+38578G>A
|
ENSP00000292538.4:n.1255+38578G>A
|
|
|
ENST00000360264.7:c.3596G>A
|
ENSP00000353401.3:p.Trp1199Ter
|
|
|
ENST00000393824.7:c.1138+38578G>A
|
ENSP00000377410.3:n.1138+38578G>A
|
|
|
ENST00000425244.6:c.1117+38578G>A
|
ENSP00000409745.2:n.1117+38578G>A
|
|
|
ENST00000437600.8:c.1255+38578G>A
|
ENSP00000414091.4:n.1255+38578G>A
|
|
|
ENST00000546411.6:c.3257G>A
|
ENSP00000450125.2:p.Trp1086Ter
|
|
|
ENST00000547394.6:c.1207+38578G>A
|
ENSP00000449371.2:n.1207+38578G>A
|
|
|
ENST00000549414.6:c.3497G>A
|
ENSP00000446630.2:p.Trp1166Ter
|
|
|
ENST00000550008.6:c.3395G>A
|
ENSP00000447373.2:p.Trp1132Ter
|
|
|
ENST00000556210.1:c.3089G>A
|
ENSP00000451558.1:p.Trp1030Ter
|
|
|
ENST00000558836.5:n.1361+38578G>A
|
|
|
|
ENST00000560541.5:n.1527+38578G>A
|
|
|
|
ENST00000622516.4:c.1249+38578G>A
|
ENSP00000484760.1:n.1249+38578G>A
|
|
|
NM_001202543.1:c.3596G>A
|
NP_001189472.1:p.Trp1199Ter
|
|
|
NM_001202544.2:c.1207+38578G>A
|
NP_001189473.1:n.1207+38578G>A
|
|
|
NM_001202545.2:c.1117+38578G>A
|
NP_001189474.1:n.1117+38578G>A
|
|
|
NM_001202546.2:c.1138+38578G>A
|
NP_001189475.1:n.1138+38578G>A
|
|
|
NM_001913.4:c.1255+38578G>A
|
NP_001904.2:n.1255+38578G>A
|
|
|
NM_181500.3:c.1249+38578G>A
|
NP_852477.1:n.1249+38578G>A
|
|
|
NM_181552.3:c.3563G>A
|
NP_853530.2:p.Trp1188Ter
|
|
|
XM_005250150.1:c.3860G>A
|
XP_005250207.1:p.Trp1287Ter
|
|
|
XM_005250151.1:c.3857G>A
|
XP_005250208.1:p.Trp1286Ter
|
|
|
XM_005250154.3:c.1522+38578G>A
|
XP_005250211.1:n.1522+38578G>A
|
|
|
XM_006715854.1:c.3797G>A
|
XP_006715917.1:p.Trp1266Ter
|
|
|
XM_006715855.1:c.1516+38578G>A
|
XP_006715918.1:n.1516+38578G>A
|
|
|
XM_006715856.2:c.3530G>A
|
XP_006715919.1:p.Trp1177Ter
|
|
|
XM_011515823.1:c.3557G>A
|
XP_011514125.1:p.Trp1186Ter
|
|
|
XM_011515824.1:c.3551G>A
|
XP_011514126.1:p.Trp1184Ter
|
|
|
XM_011515825.1:c.3290G>A
|
XP_011514127.1:p.Trp1097Ter
|
|
|
XM_005250150.3:c.3860G>A
|
XP_005250207.1:p.Trp1287Ter
|
|
|
XM_006715854.2:c.3797G>A
|
XP_006715917.1:p.Trp1266Ter
|
|
|
XM_011515825.2:c.3290G>A
|
XP_011514127.1:p.Trp1097Ter
|
|
|
XM_017011760.2:c.3524G>A
|
XP_016867249.1:p.Trp1175Ter
|
|
|
XM_024446668.1:c.3551G>A
|
XP_024302436.1:p.Trp1184Ter
|
|
|
NM_181552.4:c.3563G>A
MANE Select
|
NP_853530.2:p.Trp1188Ter
|
|
|
NM_001202543.2:c.3596G>A
|
NP_001189472.1:p.Trp1199Ter
|
|
|
NM_001202544.3:c.1207+38578G>A
|
NP_001189473.1:n.1207+38578G>A
|
|
|
NM_001202545.3:c.1117+38578G>A
|
NP_001189474.1:n.1117+38578G>A
|
|
|
NM_001202546.3:c.1138+38578G>A
|
NP_001189475.1:n.1138+38578G>A
|
|
|
NM_001913.5:c.1255+38578G>A
MANE Plus Clinical
|
NP_001904.2:n.1255+38578G>A
|
|
|
NM_181500.4:c.1249+38578G>A
|
NP_852477.1:n.1249+38578G>A
|
|
