|
NM_001267550.2:c.44222C>T
MANE Select
|
NP_001254479.2:p.Thr14741Met
|
|
ENST00000589042.5:c.44222C>T
MANE Select
|
ENSP00000467141.1:p.Thr14741Met
|
|
NM_001256850.1:c.39299C>T
|
NP_001243779.1:p.Thr13100Met
|
|
NM_003319.4:c.17027C>T
|
NP_003310.4:p.Thr5676Met
|
|
NM_133378.4:c.36518C>T
|
NP_596869.4:p.Thr12173Met
|
|
NM_133432.3:c.17402C>T
|
NP_597676.3:p.Thr5801Met
|
|
NM_133437.4:c.17603C>T
|
NP_597681.4:p.Thr5868Met
|
|
ENST00000342175.10:c.17603C>T
|
ENSP00000340554.6:p.Thr5868Met
|
|
ENST00000342175.11:c.17603C>T
|
ENSP00000340554.6:p.Thr5868Met
|
|
ENST00000342992.10:c.36518C>T
|
ENSP00000343764.6:p.Thr12173Met
|
|
ENST00000342992.11:c.36518C>T
|
ENSP00000343764.6:p.Thr12173Met
|
|
ENST00000359218.10:c.17402C>T
|
ENSP00000352154.5:p.Thr5801Met
|
|
ENST00000359218.9:c.17402C>T
|
ENSP00000352154.5:p.Thr5801Met
|
|
ENST00000460472.6:c.17027C>T
|
ENSP00000434586.1:p.Thr5676Met
|
|
ENST00000591111.5:c.39299C>T
|
ENSP00000465570.1:p.Thr13100Met
|
|
ENST00000615779.4:c.39299C>T
|
ENSP00000483597.1:p.Thr13100Met
|
|
XM_011511729.1:c.43319C>T
|
XP_011510031.1:p.Thr14440Met
|
|
XM_011511730.1:c.17213C>T
|
XP_011510032.1:p.Thr5738Met
|
|
XM_011511731.1:c.17072C>T
|
XP_011510033.1:p.Thr5691Met
|
|
XM_017004819.1:c.43115C>T
|
XP_016860308.1:p.Thr14372Met
|
|
XM_017004820.1:c.38513C>T
|
XP_016860309.1:p.Thr12838Met
|
|
XM_017004821.1:c.38510C>T
|
XP_016860310.1:p.Thr12837Met
|
|
XM_017004822.1:c.35552C>T
|
XP_016860311.1:p.Thr11851Met
|
|
XM_017004823.1:c.17168C>T
|
XP_016860312.1:p.Thr5723Met
|
|
XM_024453094.1:c.38663C>T
|
XP_024308862.1:p.Thr12888Met
|
|
XM_024453095.1:c.38660C>T
|
XP_024308863.1:p.Thr12887Met
|
|
XM_024453096.1:c.38093C>T
|
XP_024308864.1:p.Thr12698Met
|
|
XM_024453097.1:c.35435C>T
|
XP_024308865.1:p.Thr11812Met
|
|
XM_024453098.1:c.35354C>T
|
XP_024308866.1:p.Thr11785Met
|
|
XM_024453099.1:c.17117C>T
|
XP_024308867.1:p.Thr5706Met
|
|
XM_024453100.1:c.6971C>T
|
XP_024308868.1:p.Thr2324Met
|
