|
NM_001267550.2:c.28513G>T
MANE Select
|
NP_001254479.2:p.Glu9505Ter
|
|
ENST00000589042.5:c.28513G>T
MANE Select
|
ENSP00000467141.1:p.Glu9505Ter
|
|
NM_001256850.1:c.27562G>T
|
NP_001243779.1:p.Glu9188Ter
|
|
NM_003319.4:c.13282+28276G>T
|
NP_003310.4:n.13282+28276G>T
|
|
NM_133378.4:c.24781G>T
|
NP_596869.4:p.Glu8261Ter
|
|
NM_133432.3:c.13657+28276G>T
|
NP_597676.3:n.13657+28276G>T
|
|
NM_133437.4:c.13858+28276G>T
|
NP_597681.4:n.13858+28276G>T
|
|
ENST00000342175.10:c.13858+28276G>T
|
ENSP00000340554.6:n.13858+28276G>T
|
|
ENST00000342175.11:c.13858+28276G>T
|
ENSP00000340554.6:n.13858+28276G>T
|
|
ENST00000342992.10:c.24781G>T
|
ENSP00000343764.6:p.Glu8261Ter
|
|
ENST00000342992.11:c.24781G>T
|
ENSP00000343764.6:p.Glu8261Ter
|
|
ENST00000359218.10:c.13657+28276G>T
|
ENSP00000352154.5:n.13657+28276G>T
|
|
ENST00000359218.9:c.13657+28276G>T
|
ENSP00000352154.5:n.13657+28276G>T
|
|
ENST00000460472.6:c.13282+28276G>T
|
ENSP00000434586.1:n.13282+28276G>T
|
|
ENST00000591111.5:c.27562G>T
|
ENSP00000465570.1:p.Glu9188Ter
|
|
ENST00000615779.4:c.27562G>T
|
ENSP00000483597.1:p.Glu9188Ter
|
|
XM_011511729.1:c.27610G>T
|
XP_011510031.1:p.Glu9204Ter
|
|
XM_011511730.1:c.13468+28276G>T
|
XP_011510032.1:n.13468+28276G>T
|
|
XM_011511731.1:c.13327+28276G>T
|
XP_011510033.1:n.13327+28276G>T
|
|
XM_017004819.1:c.27565G>T
|
XP_016860308.1:p.Glu9189Ter
|
|
XM_017004820.1:c.24784G>T
|
XP_016860309.1:p.Glu8262Ter
|
|
XM_017004821.1:c.24781G>T
|
XP_016860310.1:p.Glu8261Ter
|
|
XM_017004822.1:c.27565G>T
|
XP_016860311.1:p.Glu9189Ter
|
|
XM_017004823.1:c.13423+28276G>T
|
XP_016860312.1:n.13423+28276G>T
|
|
XM_024453094.1:c.27565G>T
|
XP_024308862.1:p.Glu9189Ter
|
|
XM_024453095.1:c.27565G>T
|
XP_024308863.1:p.Glu9189Ter
|
|
XM_024453096.1:c.27565G>T
|
XP_024308864.1:p.Glu9189Ter
|
|
XM_024453097.1:c.27565G>T
|
XP_024308865.1:p.Glu9189Ter
|
|
XM_024453098.1:c.27565G>T
|
XP_024308866.1:p.Glu9189Ter
|
|
XM_024453099.1:c.13423+28276G>T
|
XP_024308867.1:n.13423+28276G>T
|
