ENST00000342992.11:c.88198A>G
(TTN)
|
ENSP00000343764.6:p.Thr29400Ala
|
|
ENST00000342175.11:c.69283A>G
(TTN)
|
ENSP00000340554.6:p.Thr23095Ala
|
|
ENST00000359218.10:c.69082A>G
(TTN)
|
ENSP00000352154.5:p.Thr23028Ala
|
|
ENST00000342175.10:c.69283A>G
(TTN)
|
ENSP00000340554.6:p.Thr23095Ala
|
|
ENST00000342992.10:c.88198A>G
(TTN)
|
ENSP00000343764.6:p.Thr29400Ala
|
|
ENST00000359218.9:c.69082A>G
(TTN)
|
ENSP00000352154.5:p.Thr23028Ala
|
|
ENST00000460472.6:c.68707A>G
(TTN)
|
ENSP00000434586.1:p.Thr22903Ala
|
|
ENST00000589042.5:c.95902A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31968Ala
|
|
ENST00000591111.5:c.90979A>G
(TTN)
|
ENSP00000465570.1:p.Thr30327Ala
|
|
ENST00000615779.4:c.90979A>G
(TTN)
|
ENSP00000483597.1:p.Thr30327Ala
|
|
NM_001256850.1:c.90979A>G
(TTN)
|
NP_001243779.1:p.Thr30327Ala
|
|
NM_001267550.2:c.95902A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31968Ala
|
|
NM_003319.4:c.68707A>G
(TTN)
|
NP_003310.4:p.Thr22903Ala
|
|
NM_133378.4:c.88198A>G
(TTN)
|
NP_596869.4:p.Thr29400Ala
|
|
NM_133432.3:c.69082A>G
(TTN)
|
NP_597676.3:p.Thr23028Ala
|
|
NM_133437.4:c.69283A>G
(TTN)
|
NP_597681.4:p.Thr23095Ala
|
|
NR_038271.1:n.446+20691T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1966T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.94999A>G
(TTN)
|
XP_011510031.1:p.Thr31667Ala
|
|
XM_011511730.1:c.68893A>G
(TTN)
|
XP_011510032.1:p.Thr22965Ala
|
|
XM_011511731.1:c.68752A>G
(TTN)
|
XP_011510033.1:p.Thr22918Ala
|
|
XM_017004819.1:c.94795A>G
(TTN)
|
XP_016860308.1:p.Thr31599Ala
|
|
XM_017004820.1:c.90193A>G
(TTN)
|
XP_016860309.1:p.Thr30065Ala
|
|
XM_017004821.1:c.90190A>G
(TTN)
|
XP_016860310.1:p.Thr30064Ala
|
|
XM_017004822.1:c.87232A>G
(TTN)
|
XP_016860311.1:p.Thr29078Ala
|
|
XM_017004823.1:c.68848A>G
(TTN)
|
XP_016860312.1:p.Thr22950Ala
|
|
XM_024453094.1:c.90343A>G
(TTN)
|
XP_024308862.1:p.Thr30115Ala
|
|
XM_024453095.1:c.90340A>G
(TTN)
|
XP_024308863.1:p.Thr30114Ala
|
|
XM_024453096.1:c.89773A>G
(TTN)
|
XP_024308864.1:p.Thr29925Ala
|
|
XM_024453097.1:c.87115A>G
(TTN)
|
XP_024308865.1:p.Thr29039Ala
|
|
XM_024453098.1:c.87034A>G
(TTN)
|
XP_024308866.1:p.Thr29012Ala
|
|
XM_024453099.1:c.68797A>G
(TTN)
|
XP_024308867.1:p.Thr22933Ala
|
|
XM_024453100.1:c.58651A>G
(TTN)
|
XP_024308868.1:p.Thr19551Ala
|
|