ENST00000354674.5:c.1795T>C
MANE Plus Clinical
|
ENSP00000346701.4:p.Trp599Arg
|
|
ENST00000367255.10:c.25261T>C
MANE Select
|
ENSP00000356224.5:p.Trp8421Arg
|
|
ENST00000423061.6:c.25117T>C
|
ENSP00000396024.1:p.Trp8373Arg
|
|
ENST00000672154.1:c.663T>C
|
|
|
ENST00000672169.1:c.996T>C
|
|
|
ENST00000673173.1:c.905T>C
|
|
|
ENST00000673451.1:c.1033T>C
|
ENSP00000500189.1:p.Trp345Arg
|
|
ENST00000341594.9:c.24046T>C
|
ENSP00000341887.6:p.Trp8016Arg
|
|
ENST00000347037.9:n.2009T>C
|
|
|
ENST00000354674.4:c.1795T>C
|
ENSP00000346701.4:p.Trp599Arg
|
|
ENST00000367251.7:c.4096T>C
|
ENSP00000356220.3:p.Trp1366Arg
|
|
ENST00000367255.9:c.25261T>C
|
ENSP00000356224.5:p.Trp8421Arg
|
|
ENST00000367256.9:n.8953T>C
|
|
|
ENST00000367257.8:c.3199T>C
|
ENSP00000356226.4:p.Trp1067Arg
|
|
ENST00000409694.6:n.8845T>C
|
|
|
ENST00000423061.5:c.25117T>C
|
ENSP00000396024.1:p.Trp8373Arg
|
|
ENST00000460912.6:n.1875T>C
|
|
|
ENST00000478916.5:n.4283T>C
|
|
|
ENST00000536990.5:n.2098T>C
|
|
|
ENST00000539504.5:c.1726T>C
|
ENSP00000441052.1:p.Trp576Arg
|
|
NM_033071.3:c.25117T>C
|
NP_149062.1:p.Trp8373Arg
|
|
NM_182961.3:c.25261T>C
|
NP_892006.3:p.Trp8421Arg
|
|
XM_006715407.1:c.25366T>C
|
XP_006715470.1:p.Trp8456Arg
|
|
XM_006715408.1:c.25354T>C
|
XP_006715471.1:p.Trp8452Arg
|
|
XM_006715409.1:c.25345T>C
|
XP_006715472.1:p.Trp8449Arg
|
|
XM_006715410.1:c.25366T>C
|
XP_006715473.1:p.Trp8456Arg
|
|
XM_006715411.1:c.25315T>C
|
XP_006715474.1:p.Trp8439Arg
|
|
XM_006715412.1:c.25351T>C
|
XP_006715475.1:p.Trp8451Arg
|
|
XM_006715413.1:c.25297T>C
|
XP_006715476.1:p.Trp8433Arg
|
|
XM_006715414.1:c.25294T>C
|
XP_006715477.1:p.Trp8432Arg
|
|
XM_006715415.1:c.25297T>C
|
XP_006715478.1:p.Trp8433Arg
|
|
XM_006715416.1:c.25282T>C
|
XP_006715479.1:p.Trp8428Arg
|
|
XM_006715417.1:c.25225T>C
|
XP_006715480.1:p.Trp8409Arg
|
|
XM_006715420.1:c.25213T>C
|
XP_006715483.1:p.Trp8405Arg
|
|
XM_006715421.1:c.25210T>C
|
XP_006715484.1:p.Trp8404Arg
|
|
XM_006715422.1:c.25207T>C
|
XP_006715485.1:p.Trp8403Arg
|
|
XM_006715423.1:c.25366T>C
|
XP_006715486.1:p.Trp8456Arg
|
|
XM_006715424.1:c.25366T>C
|
XP_006715487.1:p.Trp8456Arg
|
|
XM_006715425.1:c.25297T>C
|
XP_006715488.1:p.Trp8433Arg
|
|
XM_011535641.1:c.25363T>C
|
XP_011533943.1:p.Trp8455Arg
|
|
XM_011535642.1:c.25351T>C
|
XP_011533944.1:p.Trp8451Arg
|
|
XM_011535643.1:c.25201T>C
|
XP_011533945.1:p.Trp8401Arg
|
|
XM_011535644.1:c.23641T>C
|
XP_011533946.1:p.Trp7881Arg
|
|
XM_011535645.1:c.23134T>C
|
XP_011533947.1:p.Trp7712Arg
|
|
XM_011535647.1:c.18601T>C
|
XP_011533949.1:p.Trp6201Arg
|
|
NM_001347701.1:c.1867T>C
|
NP_001334630.1:p.Trp623Arg
|
|
NM_001347702.1:c.1795T>C
|
NP_001334631.1:p.Trp599Arg
|
|
XM_006715408.2:c.25354T>C
|
XP_006715471.1:p.Trp8452Arg
|
|
XM_006715410.2:c.25366T>C
|
XP_006715473.1:p.Trp8456Arg
|
|
XM_006715412.2:c.25351T>C
|
XP_006715475.1:p.Trp8451Arg
|
|
XM_006715413.2:c.25297T>C
|
XP_006715476.1:p.Trp8433Arg
|
|
XM_006715415.2:c.25297T>C
|
XP_006715478.1:p.Trp8433Arg
|
|
XM_006715416.2:c.25282T>C
|
XP_006715479.1:p.Trp8428Arg
|
|
XM_006715417.2:c.25225T>C
|
XP_006715480.1:p.Trp8409Arg
|
|
XM_006715420.2:c.25213T>C
|
XP_006715483.1:p.Trp8405Arg
|
|
XM_006715421.2:c.25210T>C
|
XP_006715484.1:p.Trp8404Arg
|
|
XM_006715423.2:c.25366T>C
|
XP_006715486.1:p.Trp8456Arg
|
|
XM_006715424.2:c.25366T>C
|
XP_006715487.1:p.Trp8456Arg
|
|
XM_006715425.2:c.25297T>C
|
XP_006715488.1:p.Trp8433Arg
|
|
XM_011535641.2:c.25363T>C
|
XP_011533943.1:p.Trp8455Arg
|
|
XM_011535642.2:c.25351T>C
|
XP_011533944.1:p.Trp8451Arg
|
|
XM_011535645.2:c.23134T>C
|
XP_011533947.1:p.Trp7712Arg
|
|
XM_017010608.1:c.25366T>C
|
XP_016866097.1:p.Trp8456Arg
|
|
XM_017010609.1:c.25366T>C
|
XP_016866098.1:p.Trp8456Arg
|
|
XM_017010610.1:c.25345T>C
|
XP_016866099.1:p.Trp8449Arg
|
|
XM_017010611.2:c.25339T>C
|
XP_016866100.1:p.Trp8447Arg
|
|
XM_017010612.1:c.25288T>C
|
XP_016866101.1:p.Trp8430Arg
|
|
XM_017010613.1:c.25294T>C
|
XP_016866102.1:p.Trp8432Arg
|
|
XM_017010614.1:c.25210T>C
|
XP_016866103.1:p.Trp8404Arg
|
|
XM_017010615.1:c.25141T>C
|
XP_016866104.1:p.Trp8381Arg
|
|
XM_017010616.1:c.25297T>C
|
XP_016866105.1:p.Trp8433Arg
|
|
XM_017010617.1:c.25294T>C
|
XP_016866106.1:p.Trp8432Arg
|
|
XM_017010618.1:c.25282T>C
|
XP_016866107.1:p.Trp8428Arg
|
|
XM_017010619.1:c.23641T>C
|
XP_016866108.1:p.Trp7881Arg
|
|
NM_182961.4:c.25261T>C
MANE Select
|
NP_892006.3:p.Trp8421Arg
|
|
NM_001347701.2:c.1867T>C
|
NP_001334630.1:p.Trp623Arg
|
|
NM_001347702.2:c.1795T>C
MANE Plus Clinical
|
NP_001334631.1:p.Trp599Arg
|
|
NM_033071.5:c.25117T>C
|
NP_149062.2:p.Trp8373Arg
|
|