|
NM_001267550.2:c.41328A>T
MANE Select
|
NP_001254479.2:p.Glu13776Asp
|
|
ENST00000589042.5:c.41328A>T
MANE Select
|
ENSP00000467141.1:p.Glu13776Asp
|
|
NM_001256850.1:c.36405A>T
|
NP_001243779.1:p.Glu12135Asp
|
|
NM_003319.4:c.14133A>T
|
NP_003310.4:p.Glu4711Asp
|
|
NM_133378.4:c.33624A>T
|
NP_596869.4:p.Glu11208Asp
|
|
NM_133432.3:c.14508A>T
|
NP_597676.3:p.Glu4836Asp
|
|
NM_133437.4:c.14709A>T
|
NP_597681.4:p.Glu4903Asp
|
|
ENST00000342175.10:c.14709A>T
|
ENSP00000340554.6:p.Glu4903Asp
|
|
ENST00000342175.11:c.14709A>T
|
ENSP00000340554.6:p.Glu4903Asp
|
|
ENST00000342992.10:c.33624A>T
|
ENSP00000343764.6:p.Glu11208Asp
|
|
ENST00000342992.11:c.33624A>T
|
ENSP00000343764.6:p.Glu11208Asp
|
|
ENST00000359218.10:c.14508A>T
|
ENSP00000352154.5:p.Glu4836Asp
|
|
ENST00000359218.9:c.14508A>T
|
ENSP00000352154.5:p.Glu4836Asp
|
|
ENST00000460472.6:c.14133A>T
|
ENSP00000434586.1:p.Glu4711Asp
|
|
ENST00000591111.5:c.36405A>T
|
ENSP00000465570.1:p.Glu12135Asp
|
|
ENST00000615779.4:c.36405A>T
|
ENSP00000483597.1:p.Glu12135Asp
|
|
XM_011511729.1:c.40425A>T
|
XP_011510031.1:p.Glu13475Asp
|
|
XM_011511730.1:c.14319A>T
|
XP_011510032.1:p.Glu4773Asp
|
|
XM_011511731.1:c.14178A>T
|
XP_011510033.1:p.Glu4726Asp
|
|
XM_017004819.1:c.40221A>T
|
XP_016860308.1:p.Glu13407Asp
|
|
XM_017004820.1:c.35619A>T
|
XP_016860309.1:p.Glu11873Asp
|
|
XM_017004821.1:c.35616A>T
|
XP_016860310.1:p.Glu11872Asp
|
|
XM_017004822.1:c.32658A>T
|
XP_016860311.1:p.Glu10886Asp
|
|
XM_017004823.1:c.14274A>T
|
XP_016860312.1:p.Glu4758Asp
|
|
XM_024453094.1:c.35769A>T
|
XP_024308862.1:p.Glu11923Asp
|
|
XM_024453095.1:c.35766A>T
|
XP_024308863.1:p.Glu11922Asp
|
|
XM_024453096.1:c.35199A>T
|
XP_024308864.1:p.Glu11733Asp
|
|
XM_024453097.1:c.32541A>T
|
XP_024308865.1:p.Glu10847Asp
|
|
XM_024453098.1:c.32460A>T
|
XP_024308866.1:p.Glu10820Asp
|
|
XM_024453099.1:c.14223A>T
|
XP_024308867.1:p.Glu4741Asp
|
|
XM_024453100.1:c.4077A>T
|
XP_024308868.1:p.Glu1359Asp
|
