ENST00000342992.11:c.59920A>T
(TTN)
|
ENSP00000343764.6:p.Arg19974Trp
|
|
ENST00000342175.11:c.41005A>T
(TTN)
|
ENSP00000340554.6:p.Arg13669Trp
|
|
ENST00000359218.10:c.40804A>T
(TTN)
|
ENSP00000352154.5:p.Arg13602Trp
|
|
ENST00000342175.10:c.41005A>T
(TTN)
|
ENSP00000340554.6:p.Arg13669Trp
|
|
ENST00000342992.10:c.59920A>T
(TTN)
|
ENSP00000343764.6:p.Arg19974Trp
|
|
ENST00000359218.9:c.40804A>T
(TTN)
|
ENSP00000352154.5:p.Arg13602Trp
|
|
ENST00000460472.6:c.40429A>T
(TTN)
|
ENSP00000434586.1:p.Arg13477Trp
|
|
ENST00000589042.5:c.67624A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg22542Trp
|
|
ENST00000591111.5:c.62701A>T
(TTN)
|
ENSP00000465570.1:p.Arg20901Trp
|
|
ENST00000615779.4:c.62701A>T
(TTN)
|
ENSP00000483597.1:p.Arg20901Trp
|
|
NM_001256850.1:c.62701A>T
(TTN)
|
NP_001243779.1:p.Arg20901Trp
|
|
NM_001267550.2:c.67624A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Arg22542Trp
|
|
NM_003319.4:c.40429A>T
(TTN)
|
NP_003310.4:p.Arg13477Trp
|
|
NM_133378.4:c.59920A>T
(TTN)
|
NP_596869.4:p.Arg19974Trp
|
|
NM_133432.3:c.40804A>T
(TTN)
|
NP_597676.3:p.Arg13602Trp
|
|
NM_133437.4:c.41005A>T
(TTN)
|
NP_597681.4:p.Arg13669Trp
|
|
NR_038271.1:n.596+8124T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-2999T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.66721A>T
(TTN)
|
XP_011510031.1:p.Arg22241Trp
|
|
XM_011511730.1:c.40615A>T
(TTN)
|
XP_011510032.1:p.Arg13539Trp
|
|
XM_011511731.1:c.40474A>T
(TTN)
|
XP_011510033.1:p.Arg13492Trp
|
|
XM_017004819.1:c.66517A>T
(TTN)
|
XP_016860308.1:p.Arg22173Trp
|
|
XM_017004820.1:c.61915A>T
(TTN)
|
XP_016860309.1:p.Arg20639Trp
|
|
XM_017004821.1:c.61912A>T
(TTN)
|
XP_016860310.1:p.Arg20638Trp
|
|
XM_017004822.1:c.58954A>T
(TTN)
|
XP_016860311.1:p.Arg19652Trp
|
|
XM_017004823.1:c.40570A>T
(TTN)
|
XP_016860312.1:p.Arg13524Trp
|
|
XM_024453094.1:c.62065A>T
(TTN)
|
XP_024308862.1:p.Arg20689Trp
|
|
XM_024453095.1:c.62062A>T
(TTN)
|
XP_024308863.1:p.Arg20688Trp
|
|
XM_024453096.1:c.61495A>T
(TTN)
|
XP_024308864.1:p.Arg20499Trp
|
|
XM_024453097.1:c.58837A>T
(TTN)
|
XP_024308865.1:p.Arg19613Trp
|
|
XM_024453098.1:c.58756A>T
(TTN)
|
XP_024308866.1:p.Arg19586Trp
|
|
XM_024453099.1:c.40519A>T
(TTN)
|
XP_024308867.1:p.Arg13507Trp
|
|
XM_024453100.1:c.30373A>T
(TTN)
|
XP_024308868.1:p.Arg10125Trp
|
|