ENST00000342992.11:c.98684G>T
(TTN)
|
ENSP00000343764.6:p.Gly32895Val
|
|
ENST00000342175.11:c.79769G>T
(TTN)
|
ENSP00000340554.6:p.Gly26590Val
|
|
ENST00000359218.10:c.79568G>T
(TTN)
|
ENSP00000352154.5:p.Gly26523Val
|
|
ENST00000342175.10:c.79769G>T
(TTN)
|
ENSP00000340554.6:p.Gly26590Val
|
|
ENST00000342992.10:c.98684G>T
(TTN)
|
ENSP00000343764.6:p.Gly32895Val
|
|
ENST00000359218.9:c.79568G>T
(TTN)
|
ENSP00000352154.5:p.Gly26523Val
|
|
ENST00000460472.6:c.79193G>T
(TTN)
|
ENSP00000434586.1:p.Gly26398Val
|
|
ENST00000589042.5:c.106388G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35463Val
|
|
ENST00000591111.5:c.101465G>T
(TTN)
|
ENSP00000465570.1:p.Gly33822Val
|
|
ENST00000615779.4:c.101465G>T
(TTN)
|
ENSP00000483597.1:p.Gly33822Val
|
|
NM_001256850.1:c.101465G>T
(TTN)
|
NP_001243779.1:p.Gly33822Val
|
|
NM_001267550.2:c.106388G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35463Val
|
|
NM_003319.4:c.79193G>T
(TTN)
|
NP_003310.4:p.Gly26398Val
|
|
NM_133378.4:c.98684G>T
(TTN)
|
NP_596869.4:p.Gly32895Val
|
|
NM_133432.3:c.79568G>T
(TTN)
|
NP_597676.3:p.Gly26523Val
|
|
NM_133437.4:c.79769G>T
(TTN)
|
NP_597681.4:p.Gly26590Val
|
|
NR_038271.1:n.446+6467C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5629C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105485G>T
(TTN)
|
XP_011510031.1:p.Gly35162Val
|
|
XM_011511730.1:c.79379G>T
(TTN)
|
XP_011510032.1:p.Gly26460Val
|
|
XM_011511731.1:c.79238G>T
(TTN)
|
XP_011510033.1:p.Gly26413Val
|
|
XM_017004819.1:c.105281G>T
(TTN)
|
XP_016860308.1:p.Gly35094Val
|
|
XM_017004820.1:c.100679G>T
(TTN)
|
XP_016860309.1:p.Gly33560Val
|
|
XM_017004821.1:c.100676G>T
(TTN)
|
XP_016860310.1:p.Gly33559Val
|
|
XM_017004822.1:c.97718G>T
(TTN)
|
XP_016860311.1:p.Gly32573Val
|
|
XM_017004823.1:c.79334G>T
(TTN)
|
XP_016860312.1:p.Gly26445Val
|
|
XM_024453094.1:c.100829G>T
(TTN)
|
XP_024308862.1:p.Gly33610Val
|
|
XM_024453095.1:c.100826G>T
(TTN)
|
XP_024308863.1:p.Gly33609Val
|
|
XM_024453096.1:c.100259G>T
(TTN)
|
XP_024308864.1:p.Gly33420Val
|
|
XM_024453097.1:c.97601G>T
(TTN)
|
XP_024308865.1:p.Gly32534Val
|
|
XM_024453098.1:c.97520G>T
(TTN)
|
XP_024308866.1:p.Gly32507Val
|
|
XM_024453099.1:c.79283G>T
(TTN)
|
XP_024308867.1:p.Gly26428Val
|
|
XM_024453100.1:c.69137G>T
(TTN)
|
XP_024308868.1:p.Gly23046Val
|
|