ENST00000342992.11:c.86341C>T
(TTN)
|
ENSP00000343764.6:p.Arg28781Cys
|
|
ENST00000342175.11:c.67426C>T
(TTN)
|
ENSP00000340554.6:p.Arg22476Cys
|
|
ENST00000359218.10:c.67225C>T
(TTN)
|
ENSP00000352154.5:p.Arg22409Cys
|
|
ENST00000342175.10:c.67426C>T
(TTN)
|
ENSP00000340554.6:p.Arg22476Cys
|
|
ENST00000342992.10:c.86341C>T
(TTN)
|
ENSP00000343764.6:p.Arg28781Cys
|
|
ENST00000359218.9:c.67225C>T
(TTN)
|
ENSP00000352154.5:p.Arg22409Cys
|
|
ENST00000460472.6:c.66850C>T
(TTN)
|
ENSP00000434586.1:p.Arg22284Cys
|
|
ENST00000589042.5:c.94045C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg31349Cys
|
|
ENST00000591111.5:c.89122C>T
(TTN)
|
ENSP00000465570.1:p.Arg29708Cys
|
|
ENST00000615779.4:c.89122C>T
(TTN)
|
ENSP00000483597.1:p.Arg29708Cys
|
|
NM_001256850.1:c.89122C>T
(TTN)
|
NP_001243779.1:p.Arg29708Cys
|
|
NM_001267550.2:c.94045C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Arg31349Cys
|
|
NM_003319.4:c.66850C>T
(TTN)
|
NP_003310.4:p.Arg22284Cys
|
|
NM_133378.4:c.86341C>T
(TTN)
|
NP_596869.4:p.Arg28781Cys
|
|
NM_133432.3:c.67225C>T
(TTN)
|
NP_597676.3:p.Arg22409Cys
|
|
NM_133437.4:c.67426C>T
(TTN)
|
NP_597681.4:p.Arg22476Cys
|
|
NR_038271.1:n.447-23719G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+5220G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.93142C>T
(TTN)
|
XP_011510031.1:p.Arg31048Cys
|
|
XM_011511730.1:c.67036C>T
(TTN)
|
XP_011510032.1:p.Arg22346Cys
|
|
XM_011511731.1:c.66895C>T
(TTN)
|
XP_011510033.1:p.Arg22299Cys
|
|
XM_017004819.1:c.92938C>T
(TTN)
|
XP_016860308.1:p.Arg30980Cys
|
|
XM_017004820.1:c.88336C>T
(TTN)
|
XP_016860309.1:p.Arg29446Cys
|
|
XM_017004821.1:c.88333C>T
(TTN)
|
XP_016860310.1:p.Arg29445Cys
|
|
XM_017004822.1:c.85375C>T
(TTN)
|
XP_016860311.1:p.Arg28459Cys
|
|
XM_017004823.1:c.66991C>T
(TTN)
|
XP_016860312.1:p.Arg22331Cys
|
|
XM_024453094.1:c.88486C>T
(TTN)
|
XP_024308862.1:p.Arg29496Cys
|
|
XM_024453095.1:c.88483C>T
(TTN)
|
XP_024308863.1:p.Arg29495Cys
|
|
XM_024453096.1:c.87916C>T
(TTN)
|
XP_024308864.1:p.Arg29306Cys
|
|
XM_024453097.1:c.85258C>T
(TTN)
|
XP_024308865.1:p.Arg28420Cys
|
|
XM_024453098.1:c.85177C>T
(TTN)
|
XP_024308866.1:p.Arg28393Cys
|
|
XM_024453099.1:c.66940C>T
(TTN)
|
XP_024308867.1:p.Arg22314Cys
|
|
XM_024453100.1:c.56794C>T
(TTN)
|
XP_024308868.1:p.Arg18932Cys
|
|