ENST00000342992.11:c.69580A>G
(TTN)
|
ENSP00000343764.6:p.Thr23194Ala
|
|
ENST00000342175.11:c.50665A>G
(TTN)
|
ENSP00000340554.6:p.Thr16889Ala
|
|
ENST00000359218.10:c.50464A>G
(TTN)
|
ENSP00000352154.5:p.Thr16822Ala
|
|
ENST00000342175.10:c.50665A>G
(TTN)
|
ENSP00000340554.6:p.Thr16889Ala
|
|
ENST00000342992.10:c.69580A>G
(TTN)
|
ENSP00000343764.6:p.Thr23194Ala
|
|
ENST00000359218.9:c.50464A>G
(TTN)
|
ENSP00000352154.5:p.Thr16822Ala
|
|
ENST00000460472.6:c.50089A>G
(TTN)
|
ENSP00000434586.1:p.Thr16697Ala
|
|
ENST00000589042.5:c.77284A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr25762Ala
|
|
ENST00000591111.5:c.72361A>G
(TTN)
|
ENSP00000465570.1:p.Thr24121Ala
|
|
ENST00000615779.4:c.72361A>G
(TTN)
|
ENSP00000483597.1:p.Thr24121Ala
|
|
NM_001256850.1:c.72361A>G
(TTN)
|
NP_001243779.1:p.Thr24121Ala
|
|
NM_001267550.2:c.77284A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr25762Ala
|
|
NM_003319.4:c.50089A>G
(TTN)
|
NP_003310.4:p.Thr16697Ala
|
|
NM_133378.4:c.69580A>G
(TTN)
|
NP_596869.4:p.Thr23194Ala
|
|
NM_133432.3:c.50464A>G
(TTN)
|
NP_597676.3:p.Thr16822Ala
|
|
NM_133437.4:c.50665A>G
(TTN)
|
NP_597681.4:p.Thr16889Ala
|
|
NR_038271.1:n.447-2452T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13724T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.76381A>G
(TTN)
|
XP_011510031.1:p.Thr25461Ala
|
|
XM_011511730.1:c.50275A>G
(TTN)
|
XP_011510032.1:p.Thr16759Ala
|
|
XM_011511731.1:c.50134A>G
(TTN)
|
XP_011510033.1:p.Thr16712Ala
|
|
XM_017004819.1:c.76177A>G
(TTN)
|
XP_016860308.1:p.Thr25393Ala
|
|
XM_017004820.1:c.71575A>G
(TTN)
|
XP_016860309.1:p.Thr23859Ala
|
|
XM_017004821.1:c.71572A>G
(TTN)
|
XP_016860310.1:p.Thr23858Ala
|
|
XM_017004822.1:c.68614A>G
(TTN)
|
XP_016860311.1:p.Thr22872Ala
|
|
XM_017004823.1:c.50230A>G
(TTN)
|
XP_016860312.1:p.Thr16744Ala
|
|
XM_024453094.1:c.71725A>G
(TTN)
|
XP_024308862.1:p.Thr23909Ala
|
|
XM_024453095.1:c.71722A>G
(TTN)
|
XP_024308863.1:p.Thr23908Ala
|
|
XM_024453096.1:c.71155A>G
(TTN)
|
XP_024308864.1:p.Thr23719Ala
|
|
XM_024453097.1:c.68497A>G
(TTN)
|
XP_024308865.1:p.Thr22833Ala
|
|
XM_024453098.1:c.68416A>G
(TTN)
|
XP_024308866.1:p.Thr22806Ala
|
|
XM_024453099.1:c.50179A>G
(TTN)
|
XP_024308867.1:p.Thr16727Ala
|
|
XM_024453100.1:c.40033A>G
(TTN)
|
XP_024308868.1:p.Thr13345Ala
|
|