|
NM_001267550.2:c.43319G>A
MANE Select
|
NP_001254479.2:p.Trp14440Ter
|
|
ENST00000589042.5:c.43319G>A
MANE Select
|
ENSP00000467141.1:p.Trp14440Ter
|
|
NM_001256850.1:c.38396G>A
|
NP_001243779.1:p.Trp12799Ter
|
|
NM_003319.4:c.16124G>A
|
NP_003310.4:p.Trp5375Ter
|
|
NM_133378.4:c.35615G>A
|
NP_596869.4:p.Trp11872Ter
|
|
NM_133432.3:c.16499G>A
|
NP_597676.3:p.Trp5500Ter
|
|
NM_133437.4:c.16700G>A
|
NP_597681.4:p.Trp5567Ter
|
|
ENST00000342175.10:c.16700G>A
|
ENSP00000340554.6:p.Trp5567Ter
|
|
ENST00000342175.11:c.16700G>A
|
ENSP00000340554.6:p.Trp5567Ter
|
|
ENST00000342992.10:c.35615G>A
|
ENSP00000343764.6:p.Trp11872Ter
|
|
ENST00000342992.11:c.35615G>A
|
ENSP00000343764.6:p.Trp11872Ter
|
|
ENST00000359218.10:c.16499G>A
|
ENSP00000352154.5:p.Trp5500Ter
|
|
ENST00000359218.9:c.16499G>A
|
ENSP00000352154.5:p.Trp5500Ter
|
|
ENST00000460472.6:c.16124G>A
|
ENSP00000434586.1:p.Trp5375Ter
|
|
ENST00000591111.5:c.38396G>A
|
ENSP00000465570.1:p.Trp12799Ter
|
|
ENST00000615779.4:c.38396G>A
|
ENSP00000483597.1:p.Trp12799Ter
|
|
XM_011511729.1:c.42416G>A
|
XP_011510031.1:p.Trp14139Ter
|
|
XM_011511730.1:c.16310G>A
|
XP_011510032.1:p.Trp5437Ter
|
|
XM_011511731.1:c.16169G>A
|
XP_011510033.1:p.Trp5390Ter
|
|
XM_017004819.1:c.42212G>A
|
XP_016860308.1:p.Trp14071Ter
|
|
XM_017004820.1:c.37610G>A
|
XP_016860309.1:p.Trp12537Ter
|
|
XM_017004821.1:c.37607G>A
|
XP_016860310.1:p.Trp12536Ter
|
|
XM_017004822.1:c.34649G>A
|
XP_016860311.1:p.Trp11550Ter
|
|
XM_017004823.1:c.16265G>A
|
XP_016860312.1:p.Trp5422Ter
|
|
XM_024453094.1:c.37760G>A
|
XP_024308862.1:p.Trp12587Ter
|
|
XM_024453095.1:c.37757G>A
|
XP_024308863.1:p.Trp12586Ter
|
|
XM_024453096.1:c.37190G>A
|
XP_024308864.1:p.Trp12397Ter
|
|
XM_024453097.1:c.34532G>A
|
XP_024308865.1:p.Trp11511Ter
|
|
XM_024453098.1:c.34451G>A
|
XP_024308866.1:p.Trp11484Ter
|
|
XM_024453099.1:c.16214G>A
|
XP_024308867.1:p.Trp5405Ter
|
|
XM_024453100.1:c.6068G>A
|
XP_024308868.1:p.Trp2023Ter
|
