ENST00000342992.11:c.94948G>T
(TTN)
|
ENSP00000343764.6:p.Asp31650Tyr
|
|
ENST00000342175.11:c.76033G>T
(TTN)
|
ENSP00000340554.6:p.Asp25345Tyr
|
|
ENST00000359218.10:c.75832G>T
(TTN)
|
ENSP00000352154.5:p.Asp25278Tyr
|
|
ENST00000342175.10:c.76033G>T
(TTN)
|
ENSP00000340554.6:p.Asp25345Tyr
|
|
ENST00000342992.10:c.94948G>T
(TTN)
|
ENSP00000343764.6:p.Asp31650Tyr
|
|
ENST00000359218.9:c.75832G>T
(TTN)
|
ENSP00000352154.5:p.Asp25278Tyr
|
|
ENST00000460472.6:c.75457G>T
(TTN)
|
ENSP00000434586.1:p.Asp25153Tyr
|
|
ENST00000589042.5:c.102652G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp34218Tyr
|
|
ENST00000591111.5:c.97729G>T
(TTN)
|
ENSP00000465570.1:p.Asp32577Tyr
|
|
ENST00000615779.4:c.97729G>T
(TTN)
|
ENSP00000483597.1:p.Asp32577Tyr
|
|
NM_001256850.1:c.97729G>T
(TTN)
|
NP_001243779.1:p.Asp32577Tyr
|
|
NM_001267550.2:c.102652G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp34218Tyr
|
|
NM_003319.4:c.75457G>T
(TTN)
|
NP_003310.4:p.Asp25153Tyr
|
|
NM_133378.4:c.94948G>T
(TTN)
|
NP_596869.4:p.Asp31650Tyr
|
|
NM_133432.3:c.75832G>T
(TTN)
|
NP_597676.3:p.Asp25278Tyr
|
|
NM_133437.4:c.76033G>T
(TTN)
|
NP_597681.4:p.Asp25345Tyr
|
|
NR_038271.1:n.446+10327C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-1769C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.101749G>T
(TTN)
|
XP_011510031.1:p.Asp33917Tyr
|
|
XM_011511730.1:c.75643G>T
(TTN)
|
XP_011510032.1:p.Asp25215Tyr
|
|
XM_011511731.1:c.75502G>T
(TTN)
|
XP_011510033.1:p.Asp25168Tyr
|
|
XM_017004819.1:c.101545G>T
(TTN)
|
XP_016860308.1:p.Asp33849Tyr
|
|
XM_017004820.1:c.96943G>T
(TTN)
|
XP_016860309.1:p.Asp32315Tyr
|
|
XM_017004821.1:c.96940G>T
(TTN)
|
XP_016860310.1:p.Asp32314Tyr
|
|
XM_017004822.1:c.93982G>T
(TTN)
|
XP_016860311.1:p.Asp31328Tyr
|
|
XM_017004823.1:c.75598G>T
(TTN)
|
XP_016860312.1:p.Asp25200Tyr
|
|
XM_024453094.1:c.97093G>T
(TTN)
|
XP_024308862.1:p.Asp32365Tyr
|
|
XM_024453095.1:c.97090G>T
(TTN)
|
XP_024308863.1:p.Asp32364Tyr
|
|
XM_024453096.1:c.96523G>T
(TTN)
|
XP_024308864.1:p.Asp32175Tyr
|
|
XM_024453097.1:c.93865G>T
(TTN)
|
XP_024308865.1:p.Asp31289Tyr
|
|
XM_024453098.1:c.93784G>T
(TTN)
|
XP_024308866.1:p.Asp31262Tyr
|
|
XM_024453099.1:c.75547G>T
(TTN)
|
XP_024308867.1:p.Asp25183Tyr
|
|
XM_024453100.1:c.65401G>T
(TTN)
|
XP_024308868.1:p.Asp21801Tyr
|
|