ENST00000342992.11:c.98366A>G
(TTN)
|
ENSP00000343764.6:p.Tyr32789Cys
|
|
ENST00000342175.11:c.79451A>G
(TTN)
|
ENSP00000340554.6:p.Tyr26484Cys
|
|
ENST00000359218.10:c.79250A>G
(TTN)
|
ENSP00000352154.5:p.Tyr26417Cys
|
|
ENST00000342175.10:c.79451A>G
(TTN)
|
ENSP00000340554.6:p.Tyr26484Cys
|
|
ENST00000342992.10:c.98366A>G
(TTN)
|
ENSP00000343764.6:p.Tyr32789Cys
|
|
ENST00000359218.9:c.79250A>G
(TTN)
|
ENSP00000352154.5:p.Tyr26417Cys
|
|
ENST00000460472.6:c.78875A>G
(TTN)
|
ENSP00000434586.1:p.Tyr26292Cys
|
|
ENST00000589042.5:c.106070A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr35357Cys
|
|
ENST00000591111.5:c.101147A>G
(TTN)
|
ENSP00000465570.1:p.Tyr33716Cys
|
|
ENST00000615779.4:c.101147A>G
(TTN)
|
ENSP00000483597.1:p.Tyr33716Cys
|
|
NM_001256850.1:c.101147A>G
(TTN)
|
NP_001243779.1:p.Tyr33716Cys
|
|
NM_001267550.2:c.106070A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr35357Cys
|
|
NM_003319.4:c.78875A>G
(TTN)
|
NP_003310.4:p.Tyr26292Cys
|
|
NM_133378.4:c.98366A>G
(TTN)
|
NP_596869.4:p.Tyr32789Cys
|
|
NM_133432.3:c.79250A>G
(TTN)
|
NP_597676.3:p.Tyr26417Cys
|
|
NM_133437.4:c.79451A>G
(TTN)
|
NP_597681.4:p.Tyr26484Cys
|
|
NR_038271.1:n.446+6909T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5187T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105167A>G
(TTN)
|
XP_011510031.1:p.Tyr35056Cys
|
|
XM_011511730.1:c.79061A>G
(TTN)
|
XP_011510032.1:p.Tyr26354Cys
|
|
XM_011511731.1:c.78920A>G
(TTN)
|
XP_011510033.1:p.Tyr26307Cys
|
|
XM_017004819.1:c.104963A>G
(TTN)
|
XP_016860308.1:p.Tyr34988Cys
|
|
XM_017004820.1:c.100361A>G
(TTN)
|
XP_016860309.1:p.Tyr33454Cys
|
|
XM_017004821.1:c.100358A>G
(TTN)
|
XP_016860310.1:p.Tyr33453Cys
|
|
XM_017004822.1:c.97400A>G
(TTN)
|
XP_016860311.1:p.Tyr32467Cys
|
|
XM_017004823.1:c.79016A>G
(TTN)
|
XP_016860312.1:p.Tyr26339Cys
|
|
XM_024453094.1:c.100511A>G
(TTN)
|
XP_024308862.1:p.Tyr33504Cys
|
|
XM_024453095.1:c.100508A>G
(TTN)
|
XP_024308863.1:p.Tyr33503Cys
|
|
XM_024453096.1:c.99941A>G
(TTN)
|
XP_024308864.1:p.Tyr33314Cys
|
|
XM_024453097.1:c.97283A>G
(TTN)
|
XP_024308865.1:p.Tyr32428Cys
|
|
XM_024453098.1:c.97202A>G
(TTN)
|
XP_024308866.1:p.Tyr32401Cys
|
|
XM_024453099.1:c.78965A>G
(TTN)
|
XP_024308867.1:p.Tyr26322Cys
|
|
XM_024453100.1:c.68819A>G
(TTN)
|
XP_024308868.1:p.Tyr22940Cys
|
|