ENST00000354674.5:c.1796G>A
MANE Plus Clinical
|
ENSP00000346701.4:p.Trp599Ter
|
|
ENST00000367255.10:c.25262G>A
MANE Select
|
ENSP00000356224.5:p.Trp8421Ter
|
|
ENST00000423061.6:c.25118G>A
|
ENSP00000396024.1:p.Trp8373Ter
|
|
ENST00000672154.1:c.664G>A
|
|
|
ENST00000672169.1:c.997G>A
|
|
|
ENST00000673173.1:c.906G>A
|
|
|
ENST00000673451.1:c.1034G>A
|
ENSP00000500189.1:p.Trp345Ter
|
|
ENST00000341594.9:c.24047G>A
|
ENSP00000341887.6:p.Trp8016Ter
|
|
ENST00000347037.9:n.2010G>A
|
|
|
ENST00000354674.4:c.1796G>A
|
ENSP00000346701.4:p.Trp599Ter
|
|
ENST00000367251.7:c.4097G>A
|
ENSP00000356220.3:p.Trp1366Ter
|
|
ENST00000367255.9:c.25262G>A
|
ENSP00000356224.5:p.Trp8421Ter
|
|
ENST00000367256.9:n.8954G>A
|
|
|
ENST00000367257.8:c.3200G>A
|
ENSP00000356226.4:p.Trp1067Ter
|
|
ENST00000409694.6:n.8846G>A
|
|
|
ENST00000423061.5:c.25118G>A
|
ENSP00000396024.1:p.Trp8373Ter
|
|
ENST00000460912.6:n.1876G>A
|
|
|
ENST00000478916.5:n.4284G>A
|
|
|
ENST00000536990.5:n.2099G>A
|
|
|
ENST00000539504.5:c.1727G>A
|
ENSP00000441052.1:p.Trp576Ter
|
|
NM_033071.3:c.25118G>A
|
NP_149062.1:p.Trp8373Ter
|
|
NM_182961.3:c.25262G>A
|
NP_892006.3:p.Trp8421Ter
|
|
XM_006715407.1:c.25367G>A
|
XP_006715470.1:p.Trp8456Ter
|
|
XM_006715408.1:c.25355G>A
|
XP_006715471.1:p.Trp8452Ter
|
|
XM_006715409.1:c.25346G>A
|
XP_006715472.1:p.Trp8449Ter
|
|
XM_006715410.1:c.25367G>A
|
XP_006715473.1:p.Trp8456Ter
|
|
XM_006715411.1:c.25316G>A
|
XP_006715474.1:p.Trp8439Ter
|
|
XM_006715412.1:c.25352G>A
|
XP_006715475.1:p.Trp8451Ter
|
|
XM_006715413.1:c.25298G>A
|
XP_006715476.1:p.Trp8433Ter
|
|
XM_006715414.1:c.25295G>A
|
XP_006715477.1:p.Trp8432Ter
|
|
XM_006715415.1:c.25298G>A
|
XP_006715478.1:p.Trp8433Ter
|
|
XM_006715416.1:c.25283G>A
|
XP_006715479.1:p.Trp8428Ter
|
|
XM_006715417.1:c.25226G>A
|
XP_006715480.1:p.Trp8409Ter
|
|
XM_006715420.1:c.25214G>A
|
XP_006715483.1:p.Trp8405Ter
|
|
XM_006715421.1:c.25211G>A
|
XP_006715484.1:p.Trp8404Ter
|
|
XM_006715422.1:c.25208G>A
|
XP_006715485.1:p.Trp8403Ter
|
|
XM_006715423.1:c.25367G>A
|
XP_006715486.1:p.Trp8456Ter
|
|
XM_006715424.1:c.25367G>A
|
XP_006715487.1:p.Trp8456Ter
|
|
XM_006715425.1:c.25298G>A
|
XP_006715488.1:p.Trp8433Ter
|
|
XM_011535641.1:c.25364G>A
|
XP_011533943.1:p.Trp8455Ter
|
|
XM_011535642.1:c.25352G>A
|
XP_011533944.1:p.Trp8451Ter
|
|
XM_011535643.1:c.25202G>A
|
XP_011533945.1:p.Trp8401Ter
|
|
XM_011535644.1:c.23642G>A
|
XP_011533946.1:p.Trp7881Ter
|
|
XM_011535645.1:c.23135G>A
|
XP_011533947.1:p.Trp7712Ter
|
|
XM_011535647.1:c.18602G>A
|
XP_011533949.1:p.Trp6201Ter
|
|
NM_001347701.1:c.1868G>A
|
NP_001334630.1:p.Trp623Ter
|
|
NM_001347702.1:c.1796G>A
|
NP_001334631.1:p.Trp599Ter
|
|
XM_006715408.2:c.25355G>A
|
XP_006715471.1:p.Trp8452Ter
|
|
XM_006715410.2:c.25367G>A
|
XP_006715473.1:p.Trp8456Ter
|
|
XM_006715412.2:c.25352G>A
|
XP_006715475.1:p.Trp8451Ter
|
|
XM_006715413.2:c.25298G>A
|
XP_006715476.1:p.Trp8433Ter
|
|
XM_006715415.2:c.25298G>A
|
XP_006715478.1:p.Trp8433Ter
|
|
XM_006715416.2:c.25283G>A
|
XP_006715479.1:p.Trp8428Ter
|
|
XM_006715417.2:c.25226G>A
|
XP_006715480.1:p.Trp8409Ter
|
|
XM_006715420.2:c.25214G>A
|
XP_006715483.1:p.Trp8405Ter
|
|
XM_006715421.2:c.25211G>A
|
XP_006715484.1:p.Trp8404Ter
|
|
XM_006715423.2:c.25367G>A
|
XP_006715486.1:p.Trp8456Ter
|
|
XM_006715424.2:c.25367G>A
|
XP_006715487.1:p.Trp8456Ter
|
|
XM_006715425.2:c.25298G>A
|
XP_006715488.1:p.Trp8433Ter
|
|
XM_011535641.2:c.25364G>A
|
XP_011533943.1:p.Trp8455Ter
|
|
XM_011535642.2:c.25352G>A
|
XP_011533944.1:p.Trp8451Ter
|
|
XM_011535645.2:c.23135G>A
|
XP_011533947.1:p.Trp7712Ter
|
|
XM_017010608.1:c.25367G>A
|
XP_016866097.1:p.Trp8456Ter
|
|
XM_017010609.1:c.25367G>A
|
XP_016866098.1:p.Trp8456Ter
|
|
XM_017010610.1:c.25346G>A
|
XP_016866099.1:p.Trp8449Ter
|
|
XM_017010611.2:c.25340G>A
|
XP_016866100.1:p.Trp8447Ter
|
|
XM_017010612.1:c.25289G>A
|
XP_016866101.1:p.Trp8430Ter
|
|
XM_017010613.1:c.25295G>A
|
XP_016866102.1:p.Trp8432Ter
|
|
XM_017010614.1:c.25211G>A
|
XP_016866103.1:p.Trp8404Ter
|
|
XM_017010615.1:c.25142G>A
|
XP_016866104.1:p.Trp8381Ter
|
|
XM_017010616.1:c.25298G>A
|
XP_016866105.1:p.Trp8433Ter
|
|
XM_017010617.1:c.25295G>A
|
XP_016866106.1:p.Trp8432Ter
|
|
XM_017010618.1:c.25283G>A
|
XP_016866107.1:p.Trp8428Ter
|
|
XM_017010619.1:c.23642G>A
|
XP_016866108.1:p.Trp7881Ter
|
|
NM_182961.4:c.25262G>A
MANE Select
|
NP_892006.3:p.Trp8421Ter
|
|
NM_001347701.2:c.1868G>A
|
NP_001334630.1:p.Trp623Ter
|
|
NM_001347702.2:c.1796G>A
MANE Plus Clinical
|
NP_001334631.1:p.Trp599Ter
|
|
NM_033071.5:c.25118G>A
|
NP_149062.2:p.Trp8373Ter
|
|