ENST00000342992.11:c.51277G>C
(TTN)
|
ENSP00000343764.6:p.Gly17093Arg
|
|
ENST00000342175.11:c.32362G>C
(TTN)
|
ENSP00000340554.6:p.Gly10788Arg
|
|
ENST00000359218.10:c.32161G>C
(TTN)
|
ENSP00000352154.5:p.Gly10721Arg
|
|
ENST00000342175.10:c.32362G>C
(TTN)
|
ENSP00000340554.6:p.Gly10788Arg
|
|
ENST00000342992.10:c.51277G>C
(TTN)
|
ENSP00000343764.6:p.Gly17093Arg
|
|
ENST00000359218.9:c.32161G>C
(TTN)
|
ENSP00000352154.5:p.Gly10721Arg
|
|
ENST00000460472.6:c.31786G>C
(TTN)
|
ENSP00000434586.1:p.Gly10596Arg
|
|
ENST00000589042.5:c.58981G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly19661Arg
|
|
ENST00000591111.5:c.54058G>C
(TTN)
|
ENSP00000465570.1:p.Gly18020Arg
|
|
ENST00000615779.4:c.54058G>C
(TTN)
|
ENSP00000483597.1:p.Gly18020Arg
|
|
NM_001256850.1:c.54058G>C
(TTN)
|
NP_001243779.1:p.Gly18020Arg
|
|
NM_001267550.2:c.58981G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly19661Arg
|
|
NM_003319.4:c.31786G>C
(TTN)
|
NP_003310.4:p.Gly10596Arg
|
|
NM_133378.4:c.51277G>C
(TTN)
|
NP_596869.4:p.Gly17093Arg
|
|
NM_133432.3:c.32161G>C
(TTN)
|
NP_597676.3:p.Gly10721Arg
|
|
NM_133437.4:c.32362G>C
(TTN)
|
NP_597681.4:p.Gly10788Arg
|
|
NR_038271.1:n.597-4369C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1913C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.58078G>C
(TTN)
|
XP_011510031.1:p.Gly19360Arg
|
|
XM_011511730.1:c.31972G>C
(TTN)
|
XP_011510032.1:p.Gly10658Arg
|
|
XM_011511731.1:c.31831G>C
(TTN)
|
XP_011510033.1:p.Gly10611Arg
|
|
XM_017004819.1:c.57874G>C
(TTN)
|
XP_016860308.1:p.Gly19292Arg
|
|
XM_017004820.1:c.53272G>C
(TTN)
|
XP_016860309.1:p.Gly17758Arg
|
|
XM_017004821.1:c.53269G>C
(TTN)
|
XP_016860310.1:p.Gly17757Arg
|
|
XM_017004822.1:c.50311G>C
(TTN)
|
XP_016860311.1:p.Gly16771Arg
|
|
XM_017004823.1:c.31927G>C
(TTN)
|
XP_016860312.1:p.Gly10643Arg
|
|
XM_024453094.1:c.53422G>C
(TTN)
|
XP_024308862.1:p.Gly17808Arg
|
|
XM_024453095.1:c.53419G>C
(TTN)
|
XP_024308863.1:p.Gly17807Arg
|
|
XM_024453096.1:c.52852G>C
(TTN)
|
XP_024308864.1:p.Gly17618Arg
|
|
XM_024453097.1:c.50194G>C
(TTN)
|
XP_024308865.1:p.Gly16732Arg
|
|
XM_024453098.1:c.50113G>C
(TTN)
|
XP_024308866.1:p.Gly16705Arg
|
|
XM_024453099.1:c.31876G>C
(TTN)
|
XP_024308867.1:p.Gly10626Arg
|
|
XM_024453100.1:c.21730G>C
(TTN)
|
XP_024308868.1:p.Gly7244Arg
|
|