|
ENST00000292535.12:c.2942dup
MANE Select
|
ENSP00000292535.7:p.Met981IlefsTer?
|
|
|
ENST00000292538.9:c.1255+8822dup
|
ENSP00000292538.4:n.1255+8822dup
|
|
|
ENST00000437600.9:c.1249+8822dup
|
ENSP00000414091.5:n.1249+8822dup
|
|
|
ENST00000546411.7:c.2942dup
|
ENSP00000450125.3:p.Met981IlefsTer?
|
|
|
ENST00000622516.6:c.1255+8822dup
MANE Plus Clinical
|
ENSP00000484760.2:n.1255+8822dup
|
|
|
ENST00000645010.1:c.2807dup
|
ENSP00000496653.1:p.Met936IlefsTer?
|
|
|
ENST00000646649.1:c.2501dup
|
ENSP00000494610.1:p.Met834IlefsTer?
|
|
|
ENST00000292535.11:c.2942dup
|
ENSP00000292535.7:p.Met981IlefsTer?
|
|
|
ENST00000292538.8:c.1255+8822dup
|
ENSP00000292538.4:n.1255+8822dup
|
|
|
ENST00000360264.7:c.2975dup
|
ENSP00000353401.3:p.Met992IlefsTer?
|
|
|
ENST00000393824.7:c.1138+8822dup
|
ENSP00000377410.3:n.1138+8822dup
|
|
|
ENST00000425244.6:c.1117+8822dup
|
ENSP00000409745.2:n.1117+8822dup
|
|
|
ENST00000437600.8:c.1255+8822dup
|
ENSP00000414091.4:n.1255+8822dup
|
|
|
ENST00000546411.6:c.2636dup
|
ENSP00000450125.2:p.Met879IlefsTer?
|
|
|
ENST00000547394.6:c.1207+8822dup
|
ENSP00000449371.2:n.1207+8822dup
|
|
|
ENST00000549414.6:c.2876dup
|
ENSP00000446630.2:p.Met959IlefsTer?
|
|
|
ENST00000550008.6:c.2774dup
|
ENSP00000447373.2:p.Met925IlefsTer?
|
|
|
ENST00000556210.1:c.2468dup
|
ENSP00000451558.1:p.Met823IlefsTer?
|
|
|
ENST00000558836.5:n.1361+8822dup
|
|
|
|
ENST00000560541.5:n.1527+8822dup
|
|
|
|
ENST00000622516.4:c.1249+8822dup
|
ENSP00000484760.1:n.1249+8822dup
|
|
|
NM_001202543.1:c.2975dup
|
NP_001189472.1:p.Met992IlefsTer?
|
|
|
NM_001202544.2:c.1207+8822dup
|
NP_001189473.1:n.1207+8822dup
|
|
|
NM_001202545.2:c.1117+8822dup
|
NP_001189474.1:n.1117+8822dup
|
|
|
NM_001202546.2:c.1138+8822dup
|
NP_001189475.1:n.1138+8822dup
|
|
|
NM_001913.4:c.1255+8822dup
|
NP_001904.2:n.1255+8822dup
|
|
|
NM_181500.3:c.1249+8822dup
|
NP_852477.1:n.1249+8822dup
|
|
|
NM_181552.3:c.2942dup
|
NP_853530.2:p.Met981IlefsTer?
|
|
|
XM_005250150.1:c.3239dup
|
XP_005250207.1:p.Met1080IlefsTer?
|
|
|
XM_005250151.1:c.3236dup
|
XP_005250208.1:p.Met1079IlefsTer?
|
|
|
XM_005250154.3:c.1522+8822dup
|
XP_005250211.1:n.1522+8822dup
|
|
|
XM_006715854.1:c.3176dup
|
XP_006715917.1:p.Met1059IlefsTer?
|
|
|
XM_006715855.1:c.1516+8822dup
|
XP_006715918.1:n.1516+8822dup
|
|
|
XM_006715856.2:c.2909dup
|
XP_006715919.1:p.Met970IlefsTer?
|
|
|
XM_011515823.1:c.2936dup
|
XP_011514125.1:p.Met979IlefsTer?
|
|
|
XM_011515824.1:c.2930dup
|
XP_011514126.1:p.Met977IlefsTer?
|
|
|
XM_011515825.1:c.2669dup
|
XP_011514127.1:p.Met890IlefsTer?
|
|
|
XM_005250150.3:c.3239dup
|
XP_005250207.1:p.Met1080IlefsTer?
|
|
|
XM_006715854.2:c.3176dup
|
XP_006715917.1:p.Met1059IlefsTer?
|
|
|
XM_011515825.2:c.2669dup
|
XP_011514127.1:p.Met890IlefsTer?
|
|
|
XM_017011760.2:c.2903dup
|
XP_016867249.1:p.Met968IlefsTer?
|
|
|
XM_024446668.1:c.2930dup
|
XP_024302436.1:p.Met977IlefsTer?
|
|
|
NM_181552.4:c.2942dup
MANE Select
|
NP_853530.2:p.Met981IlefsTer?
|
|
|
NM_001202543.2:c.2975dup
|
NP_001189472.1:p.Met992IlefsTer?
|
|
|
NM_001202544.3:c.1207+8822dup
|
NP_001189473.1:n.1207+8822dup
|
|
|
NM_001202545.3:c.1117+8822dup
|
NP_001189474.1:n.1117+8822dup
|
|
|
NM_001202546.3:c.1138+8822dup
|
NP_001189475.1:n.1138+8822dup
|
|
|
NM_001913.5:c.1255+8822dup
MANE Plus Clinical
|
NP_001904.2:n.1255+8822dup
|
|
|
NM_181500.4:c.1249+8822dup
|
NP_852477.1:n.1249+8822dup
|
|
