ENST00000342992.11:c.88531G>T
(TTN)
|
ENSP00000343764.6:p.Asp29511Tyr
|
|
ENST00000342175.11:c.69616G>T
(TTN)
|
ENSP00000340554.6:p.Asp23206Tyr
|
|
ENST00000359218.10:c.69415G>T
(TTN)
|
ENSP00000352154.5:p.Asp23139Tyr
|
|
ENST00000342175.10:c.69616G>T
(TTN)
|
ENSP00000340554.6:p.Asp23206Tyr
|
|
ENST00000342992.10:c.88531G>T
(TTN)
|
ENSP00000343764.6:p.Asp29511Tyr
|
|
ENST00000359218.9:c.69415G>T
(TTN)
|
ENSP00000352154.5:p.Asp23139Tyr
|
|
ENST00000460472.6:c.69040G>T
(TTN)
|
ENSP00000434586.1:p.Asp23014Tyr
|
|
ENST00000589042.5:c.96235G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp32079Tyr
|
|
ENST00000591111.5:c.91312G>T
(TTN)
|
ENSP00000465570.1:p.Asp30438Tyr
|
|
ENST00000615779.4:c.91312G>T
(TTN)
|
ENSP00000483597.1:p.Asp30438Tyr
|
|
NM_001256850.1:c.91312G>T
(TTN)
|
NP_001243779.1:p.Asp30438Tyr
|
|
NM_001267550.2:c.96235G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp32079Tyr
|
|
NM_003319.4:c.69040G>T
(TTN)
|
NP_003310.4:p.Asp23014Tyr
|
|
NM_133378.4:c.88531G>T
(TTN)
|
NP_596869.4:p.Asp29511Tyr
|
|
NM_133432.3:c.69415G>T
(TTN)
|
NP_597676.3:p.Asp23139Tyr
|
|
NM_133437.4:c.69616G>T
(TTN)
|
NP_597681.4:p.Asp23206Tyr
|
|
NR_038271.1:n.446+20273C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1548C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.95332G>T
(TTN)
|
XP_011510031.1:p.Asp31778Tyr
|
|
XM_011511730.1:c.69226G>T
(TTN)
|
XP_011510032.1:p.Asp23076Tyr
|
|
XM_011511731.1:c.69085G>T
(TTN)
|
XP_011510033.1:p.Asp23029Tyr
|
|
XM_017004819.1:c.95128G>T
(TTN)
|
XP_016860308.1:p.Asp31710Tyr
|
|
XM_017004820.1:c.90526G>T
(TTN)
|
XP_016860309.1:p.Asp30176Tyr
|
|
XM_017004821.1:c.90523G>T
(TTN)
|
XP_016860310.1:p.Asp30175Tyr
|
|
XM_017004822.1:c.87565G>T
(TTN)
|
XP_016860311.1:p.Asp29189Tyr
|
|
XM_017004823.1:c.69181G>T
(TTN)
|
XP_016860312.1:p.Asp23061Tyr
|
|
XM_024453094.1:c.90676G>T
(TTN)
|
XP_024308862.1:p.Asp30226Tyr
|
|
XM_024453095.1:c.90673G>T
(TTN)
|
XP_024308863.1:p.Asp30225Tyr
|
|
XM_024453096.1:c.90106G>T
(TTN)
|
XP_024308864.1:p.Asp30036Tyr
|
|
XM_024453097.1:c.87448G>T
(TTN)
|
XP_024308865.1:p.Asp29150Tyr
|
|
XM_024453098.1:c.87367G>T
(TTN)
|
XP_024308866.1:p.Asp29123Tyr
|
|
XM_024453099.1:c.69130G>T
(TTN)
|
XP_024308867.1:p.Asp23044Tyr
|
|
XM_024453100.1:c.58984G>T
(TTN)
|
XP_024308868.1:p.Asp19662Tyr
|
|