ENST00000342992.11:c.73823G>A
(TTN)
|
ENSP00000343764.6:p.Arg24608His
|
|
ENST00000342175.11:c.54908G>A
(TTN)
|
ENSP00000340554.6:p.Arg18303His
|
|
ENST00000359218.10:c.54707G>A
(TTN)
|
ENSP00000352154.5:p.Arg18236His
|
|
ENST00000342175.10:c.54908G>A
(TTN)
|
ENSP00000340554.6:p.Arg18303His
|
|
ENST00000342992.10:c.73823G>A
(TTN)
|
ENSP00000343764.6:p.Arg24608His
|
|
ENST00000359218.9:c.54707G>A
(TTN)
|
ENSP00000352154.5:p.Arg18236His
|
|
ENST00000460472.6:c.54332G>A
(TTN)
|
ENSP00000434586.1:p.Arg18111His
|
|
ENST00000589042.5:c.81527G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg27176His
|
|
ENST00000591111.5:c.76604G>A
(TTN)
|
ENSP00000465570.1:p.Arg25535His
|
|
ENST00000615779.4:c.76604G>A
(TTN)
|
ENSP00000483597.1:p.Arg25535His
|
|
NM_001256850.1:c.76604G>A
(TTN)
|
NP_001243779.1:p.Arg25535His
|
|
NM_001267550.2:c.81527G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Arg27176His
|
|
NM_003319.4:c.54332G>A
(TTN)
|
NP_003310.4:p.Arg18111His
|
|
NM_133378.4:c.73823G>A
(TTN)
|
NP_596869.4:p.Arg24608His
|
|
NM_133432.3:c.54707G>A
(TTN)
|
NP_597676.3:p.Arg18236His
|
|
NM_133437.4:c.54908G>A
(TTN)
|
NP_597681.4:p.Arg18303His
|
|
NR_038271.1:n.447-6695C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-17967C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.80624G>A
(TTN)
|
XP_011510031.1:p.Arg26875His
|
|
XM_011511730.1:c.54518G>A
(TTN)
|
XP_011510032.1:p.Arg18173His
|
|
XM_011511731.1:c.54377G>A
(TTN)
|
XP_011510033.1:p.Arg18126His
|
|
XM_017004819.1:c.80420G>A
(TTN)
|
XP_016860308.1:p.Arg26807His
|
|
XM_017004820.1:c.75818G>A
(TTN)
|
XP_016860309.1:p.Arg25273His
|
|
XM_017004821.1:c.75815G>A
(TTN)
|
XP_016860310.1:p.Arg25272His
|
|
XM_017004822.1:c.72857G>A
(TTN)
|
XP_016860311.1:p.Arg24286His
|
|
XM_017004823.1:c.54473G>A
(TTN)
|
XP_016860312.1:p.Arg18158His
|
|
XM_024453094.1:c.75968G>A
(TTN)
|
XP_024308862.1:p.Arg25323His
|
|
XM_024453095.1:c.75965G>A
(TTN)
|
XP_024308863.1:p.Arg25322His
|
|
XM_024453096.1:c.75398G>A
(TTN)
|
XP_024308864.1:p.Arg25133His
|
|
XM_024453097.1:c.72740G>A
(TTN)
|
XP_024308865.1:p.Arg24247His
|
|
XM_024453098.1:c.72659G>A
(TTN)
|
XP_024308866.1:p.Arg24220His
|
|
XM_024453099.1:c.54422G>A
(TTN)
|
XP_024308867.1:p.Arg18141His
|
|
XM_024453100.1:c.44276G>A
(TTN)
|
XP_024308868.1:p.Arg14759His
|
|