ENST00000342992.11:c.84184A>G
(TTN)
|
ENSP00000343764.6:p.Thr28062Ala
|
|
ENST00000342175.11:c.65269A>G
(TTN)
|
ENSP00000340554.6:p.Thr21757Ala
|
|
ENST00000359218.10:c.65068A>G
(TTN)
|
ENSP00000352154.5:p.Thr21690Ala
|
|
ENST00000342175.10:c.65269A>G
(TTN)
|
ENSP00000340554.6:p.Thr21757Ala
|
|
ENST00000342992.10:c.84184A>G
(TTN)
|
ENSP00000343764.6:p.Thr28062Ala
|
|
ENST00000359218.9:c.65068A>G
(TTN)
|
ENSP00000352154.5:p.Thr21690Ala
|
|
ENST00000460472.6:c.64693A>G
(TTN)
|
ENSP00000434586.1:p.Thr21565Ala
|
|
ENST00000589042.5:c.91888A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr30630Ala
|
|
ENST00000591111.5:c.86965A>G
(TTN)
|
ENSP00000465570.1:p.Thr28989Ala
|
|
ENST00000615779.4:c.86965A>G
(TTN)
|
ENSP00000483597.1:p.Thr28989Ala
|
|
NM_001256850.1:c.86965A>G
(TTN)
|
NP_001243779.1:p.Thr28989Ala
|
|
NM_001267550.2:c.91888A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr30630Ala
|
|
NM_003319.4:c.64693A>G
(TTN)
|
NP_003310.4:p.Thr21565Ala
|
|
NM_133378.4:c.84184A>G
(TTN)
|
NP_596869.4:p.Thr28062Ala
|
|
NM_133432.3:c.65068A>G
(TTN)
|
NP_597676.3:p.Thr21690Ala
|
|
NM_133437.4:c.65269A>G
(TTN)
|
NP_597681.4:p.Thr21757Ala
|
|
NR_038271.1:n.447-21466T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+7473T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.90985A>G
(TTN)
|
XP_011510031.1:p.Thr30329Ala
|
|
XM_011511730.1:c.64879A>G
(TTN)
|
XP_011510032.1:p.Thr21627Ala
|
|
XM_011511731.1:c.64738A>G
(TTN)
|
XP_011510033.1:p.Thr21580Ala
|
|
XM_017004819.1:c.90781A>G
(TTN)
|
XP_016860308.1:p.Thr30261Ala
|
|
XM_017004820.1:c.86179A>G
(TTN)
|
XP_016860309.1:p.Thr28727Ala
|
|
XM_017004821.1:c.86176A>G
(TTN)
|
XP_016860310.1:p.Thr28726Ala
|
|
XM_017004822.1:c.83218A>G
(TTN)
|
XP_016860311.1:p.Thr27740Ala
|
|
XM_017004823.1:c.64834A>G
(TTN)
|
XP_016860312.1:p.Thr21612Ala
|
|
XM_024453094.1:c.86329A>G
(TTN)
|
XP_024308862.1:p.Thr28777Ala
|
|
XM_024453095.1:c.86326A>G
(TTN)
|
XP_024308863.1:p.Thr28776Ala
|
|
XM_024453096.1:c.85759A>G
(TTN)
|
XP_024308864.1:p.Thr28587Ala
|
|
XM_024453097.1:c.83101A>G
(TTN)
|
XP_024308865.1:p.Thr27701Ala
|
|
XM_024453098.1:c.83020A>G
(TTN)
|
XP_024308866.1:p.Thr27674Ala
|
|
XM_024453099.1:c.64783A>G
(TTN)
|
XP_024308867.1:p.Thr21595Ala
|
|
XM_024453100.1:c.54637A>G
(TTN)
|
XP_024308868.1:p.Thr18213Ala
|
|