|
ENST00000292535.12:c.3551G>A
MANE Select
|
ENSP00000292535.7:p.Arg1184Gln
|
|
|
ENST00000292538.9:c.1255+38566G>A
|
ENSP00000292538.4:n.1255+38566G>A
|
|
|
ENST00000437600.9:c.1249+38566G>A
|
ENSP00000414091.5:n.1249+38566G>A
|
|
|
ENST00000546411.7:c.3551G>A
|
ENSP00000450125.3:p.Arg1184Gln
|
|
|
ENST00000622516.6:c.1255+38566G>A
MANE Plus Clinical
|
ENSP00000484760.2:n.1255+38566G>A
|
|
|
ENST00000645010.1:c.3416G>A
|
ENSP00000496653.1:p.Arg1139Gln
|
|
|
ENST00000646649.1:c.3110G>A
|
ENSP00000494610.1:p.Arg1037Gln
|
|
|
ENST00000292535.11:c.3551G>A
|
ENSP00000292535.7:p.Arg1184Gln
|
|
|
ENST00000292538.8:c.1255+38566G>A
|
ENSP00000292538.4:n.1255+38566G>A
|
|
|
ENST00000360264.7:c.3584G>A
|
ENSP00000353401.3:p.Arg1195Gln
|
|
|
ENST00000393824.7:c.1138+38566G>A
|
ENSP00000377410.3:n.1138+38566G>A
|
|
|
ENST00000425244.6:c.1117+38566G>A
|
ENSP00000409745.2:n.1117+38566G>A
|
|
|
ENST00000437600.8:c.1255+38566G>A
|
ENSP00000414091.4:n.1255+38566G>A
|
|
|
ENST00000546411.6:c.3245G>A
|
ENSP00000450125.2:p.Arg1082Gln
|
|
|
ENST00000547394.6:c.1207+38566G>A
|
ENSP00000449371.2:n.1207+38566G>A
|
|
|
ENST00000549414.6:c.3485G>A
|
ENSP00000446630.2:p.Arg1162Gln
|
|
|
ENST00000550008.6:c.3383G>A
|
ENSP00000447373.2:p.Arg1128Gln
|
|
|
ENST00000556210.1:c.3077G>A
|
ENSP00000451558.1:p.Arg1026Gln
|
|
|
ENST00000558836.5:n.1361+38566G>A
|
|
|
|
ENST00000560541.5:n.1527+38566G>A
|
|
|
|
ENST00000622516.4:c.1249+38566G>A
|
ENSP00000484760.1:n.1249+38566G>A
|
|
|
NM_001202543.1:c.3584G>A
|
NP_001189472.1:p.Arg1195Gln
|
|
|
NM_001202544.2:c.1207+38566G>A
|
NP_001189473.1:n.1207+38566G>A
|
|
|
NM_001202545.2:c.1117+38566G>A
|
NP_001189474.1:n.1117+38566G>A
|
|
|
NM_001202546.2:c.1138+38566G>A
|
NP_001189475.1:n.1138+38566G>A
|
|
|
NM_001913.4:c.1255+38566G>A
|
NP_001904.2:n.1255+38566G>A
|
|
|
NM_181500.3:c.1249+38566G>A
|
NP_852477.1:n.1249+38566G>A
|
|
|
NM_181552.3:c.3551G>A
|
NP_853530.2:p.Arg1184Gln
|
|
|
XM_005250150.1:c.3848G>A
|
XP_005250207.1:p.Arg1283Gln
|
|
|
XM_005250151.1:c.3845G>A
|
XP_005250208.1:p.Arg1282Gln
|
|
|
XM_005250154.3:c.1522+38566G>A
|
XP_005250211.1:n.1522+38566G>A
|
|
|
XM_006715854.1:c.3785G>A
|
XP_006715917.1:p.Arg1262Gln
|
|
|
XM_006715855.1:c.1516+38566G>A
|
XP_006715918.1:n.1516+38566G>A
|
|
|
XM_006715856.2:c.3518G>A
|
XP_006715919.1:p.Arg1173Gln
|
|
|
XM_011515823.1:c.3545G>A
|
XP_011514125.1:p.Arg1182Gln
|
|
|
XM_011515824.1:c.3539G>A
|
XP_011514126.1:p.Arg1180Gln
|
|
|
XM_011515825.1:c.3278G>A
|
XP_011514127.1:p.Arg1093Gln
|
|
|
XM_005250150.3:c.3848G>A
|
XP_005250207.1:p.Arg1283Gln
|
|
|
XM_006715854.2:c.3785G>A
|
XP_006715917.1:p.Arg1262Gln
|
|
|
XM_011515825.2:c.3278G>A
|
XP_011514127.1:p.Arg1093Gln
|
|
|
XM_017011760.2:c.3512G>A
|
XP_016867249.1:p.Arg1171Gln
|
|
|
XM_024446668.1:c.3539G>A
|
XP_024302436.1:p.Arg1180Gln
|
|
|
NM_181552.4:c.3551G>A
MANE Select
|
NP_853530.2:p.Arg1184Gln
|
|
|
NM_001202543.2:c.3584G>A
|
NP_001189472.1:p.Arg1195Gln
|
|
|
NM_001202544.3:c.1207+38566G>A
|
NP_001189473.1:n.1207+38566G>A
|
|
|
NM_001202545.3:c.1117+38566G>A
|
NP_001189474.1:n.1117+38566G>A
|
|
|
NM_001202546.3:c.1138+38566G>A
|
NP_001189475.1:n.1138+38566G>A
|
|
|
NM_001913.5:c.1255+38566G>A
MANE Plus Clinical
|
NP_001904.2:n.1255+38566G>A
|
|
|
NM_181500.4:c.1249+38566G>A
|
NP_852477.1:n.1249+38566G>A
|
|
