ENST00000342992.11:c.98320T>G
(TTN)
|
ENSP00000343764.6:p.Tyr32774Asp
|
|
ENST00000342175.11:c.79405T>G
(TTN)
|
ENSP00000340554.6:p.Tyr26469Asp
|
|
ENST00000359218.10:c.79204T>G
(TTN)
|
ENSP00000352154.5:p.Tyr26402Asp
|
|
ENST00000342175.10:c.79405T>G
(TTN)
|
ENSP00000340554.6:p.Tyr26469Asp
|
|
ENST00000342992.10:c.98320T>G
(TTN)
|
ENSP00000343764.6:p.Tyr32774Asp
|
|
ENST00000359218.9:c.79204T>G
(TTN)
|
ENSP00000352154.5:p.Tyr26402Asp
|
|
ENST00000460472.6:c.78829T>G
(TTN)
|
ENSP00000434586.1:p.Tyr26277Asp
|
|
ENST00000589042.5:c.106024T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr35342Asp
|
|
ENST00000591111.5:c.101101T>G
(TTN)
|
ENSP00000465570.1:p.Tyr33701Asp
|
|
ENST00000615779.4:c.101101T>G
(TTN)
|
ENSP00000483597.1:p.Tyr33701Asp
|
|
NM_001256850.1:c.101101T>G
(TTN)
|
NP_001243779.1:p.Tyr33701Asp
|
|
NM_001267550.2:c.106024T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr35342Asp
|
|
NM_003319.4:c.78829T>G
(TTN)
|
NP_003310.4:p.Tyr26277Asp
|
|
NM_133378.4:c.98320T>G
(TTN)
|
NP_596869.4:p.Tyr32774Asp
|
|
NM_133432.3:c.79204T>G
(TTN)
|
NP_597676.3:p.Tyr26402Asp
|
|
NM_133437.4:c.79405T>G
(TTN)
|
NP_597681.4:p.Tyr26469Asp
|
|
NR_038271.1:n.446+6955A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5141A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105121T>G
(TTN)
|
XP_011510031.1:p.Tyr35041Asp
|
|
XM_011511730.1:c.79015T>G
(TTN)
|
XP_011510032.1:p.Tyr26339Asp
|
|
XM_011511731.1:c.78874T>G
(TTN)
|
XP_011510033.1:p.Tyr26292Asp
|
|
XM_017004819.1:c.104917T>G
(TTN)
|
XP_016860308.1:p.Tyr34973Asp
|
|
XM_017004820.1:c.100315T>G
(TTN)
|
XP_016860309.1:p.Tyr33439Asp
|
|
XM_017004821.1:c.100312T>G
(TTN)
|
XP_016860310.1:p.Tyr33438Asp
|
|
XM_017004822.1:c.97354T>G
(TTN)
|
XP_016860311.1:p.Tyr32452Asp
|
|
XM_017004823.1:c.78970T>G
(TTN)
|
XP_016860312.1:p.Tyr26324Asp
|
|
XM_024453094.1:c.100465T>G
(TTN)
|
XP_024308862.1:p.Tyr33489Asp
|
|
XM_024453095.1:c.100462T>G
(TTN)
|
XP_024308863.1:p.Tyr33488Asp
|
|
XM_024453096.1:c.99895T>G
(TTN)
|
XP_024308864.1:p.Tyr33299Asp
|
|
XM_024453097.1:c.97237T>G
(TTN)
|
XP_024308865.1:p.Tyr32413Asp
|
|
XM_024453098.1:c.97156T>G
(TTN)
|
XP_024308866.1:p.Tyr32386Asp
|
|
XM_024453099.1:c.78919T>G
(TTN)
|
XP_024308867.1:p.Tyr26307Asp
|
|
XM_024453100.1:c.68773T>G
(TTN)
|
XP_024308868.1:p.Tyr22925Asp
|
|