|
NM_001267550.2:c.42785G>A
MANE Select
|
NP_001254479.2:p.Trp14262Ter
|
|
ENST00000589042.5:c.42785G>A
MANE Select
|
ENSP00000467141.1:p.Trp14262Ter
|
|
NM_001256850.1:c.37862G>A
|
NP_001243779.1:p.Trp12621Ter
|
|
NM_003319.4:c.15590G>A
|
NP_003310.4:p.Trp5197Ter
|
|
NM_133378.4:c.35081G>A
|
NP_596869.4:p.Trp11694Ter
|
|
NM_133432.3:c.15965G>A
|
NP_597676.3:p.Trp5322Ter
|
|
NM_133437.4:c.16166G>A
|
NP_597681.4:p.Trp5389Ter
|
|
ENST00000342175.10:c.16166G>A
|
ENSP00000340554.6:p.Trp5389Ter
|
|
ENST00000342175.11:c.16166G>A
|
ENSP00000340554.6:p.Trp5389Ter
|
|
ENST00000342992.10:c.35081G>A
|
ENSP00000343764.6:p.Trp11694Ter
|
|
ENST00000342992.11:c.35081G>A
|
ENSP00000343764.6:p.Trp11694Ter
|
|
ENST00000359218.10:c.15965G>A
|
ENSP00000352154.5:p.Trp5322Ter
|
|
ENST00000359218.9:c.15965G>A
|
ENSP00000352154.5:p.Trp5322Ter
|
|
ENST00000460472.6:c.15590G>A
|
ENSP00000434586.1:p.Trp5197Ter
|
|
ENST00000591111.5:c.37862G>A
|
ENSP00000465570.1:p.Trp12621Ter
|
|
ENST00000615779.4:c.37862G>A
|
ENSP00000483597.1:p.Trp12621Ter
|
|
XM_011511729.1:c.41882G>A
|
XP_011510031.1:p.Trp13961Ter
|
|
XM_011511730.1:c.15776G>A
|
XP_011510032.1:p.Trp5259Ter
|
|
XM_011511731.1:c.15635G>A
|
XP_011510033.1:p.Trp5212Ter
|
|
XM_017004819.1:c.41678G>A
|
XP_016860308.1:p.Trp13893Ter
|
|
XM_017004820.1:c.37076G>A
|
XP_016860309.1:p.Trp12359Ter
|
|
XM_017004821.1:c.37073G>A
|
XP_016860310.1:p.Trp12358Ter
|
|
XM_017004822.1:c.34115G>A
|
XP_016860311.1:p.Trp11372Ter
|
|
XM_017004823.1:c.15731G>A
|
XP_016860312.1:p.Trp5244Ter
|
|
XM_024453094.1:c.37226G>A
|
XP_024308862.1:p.Trp12409Ter
|
|
XM_024453095.1:c.37223G>A
|
XP_024308863.1:p.Trp12408Ter
|
|
XM_024453096.1:c.36656G>A
|
XP_024308864.1:p.Trp12219Ter
|
|
XM_024453097.1:c.33998G>A
|
XP_024308865.1:p.Trp11333Ter
|
|
XM_024453098.1:c.33917G>A
|
XP_024308866.1:p.Trp11306Ter
|
|
XM_024453099.1:c.15680G>A
|
XP_024308867.1:p.Trp5227Ter
|
|
XM_024453100.1:c.5534G>A
|
XP_024308868.1:p.Trp1845Ter
|
