ENST00000342992.11:c.69323C>G
(TTN)
|
ENSP00000343764.6:p.Thr23108Arg
|
|
ENST00000342175.11:c.50408C>G
(TTN)
|
ENSP00000340554.6:p.Thr16803Arg
|
|
ENST00000359218.10:c.50207C>G
(TTN)
|
ENSP00000352154.5:p.Thr16736Arg
|
|
ENST00000342175.10:c.50408C>G
(TTN)
|
ENSP00000340554.6:p.Thr16803Arg
|
|
ENST00000342992.10:c.69323C>G
(TTN)
|
ENSP00000343764.6:p.Thr23108Arg
|
|
ENST00000359218.9:c.50207C>G
(TTN)
|
ENSP00000352154.5:p.Thr16736Arg
|
|
ENST00000460472.6:c.49832C>G
(TTN)
|
ENSP00000434586.1:p.Thr16611Arg
|
|
ENST00000589042.5:c.77027C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr25676Arg
|
|
ENST00000591111.5:c.72104C>G
(TTN)
|
ENSP00000465570.1:p.Thr24035Arg
|
|
ENST00000615779.4:c.72104C>G
(TTN)
|
ENSP00000483597.1:p.Thr24035Arg
|
|
NM_001256850.1:c.72104C>G
(TTN)
|
NP_001243779.1:p.Thr24035Arg
|
|
NM_001267550.2:c.77027C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr25676Arg
|
|
NM_003319.4:c.49832C>G
(TTN)
|
NP_003310.4:p.Thr16611Arg
|
|
NM_133378.4:c.69323C>G
(TTN)
|
NP_596869.4:p.Thr23108Arg
|
|
NM_133432.3:c.50207C>G
(TTN)
|
NP_597676.3:p.Thr16736Arg
|
|
NM_133437.4:c.50408C>G
(TTN)
|
NP_597681.4:p.Thr16803Arg
|
|
NR_038271.1:n.447-2195G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13467G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.76124C>G
(TTN)
|
XP_011510031.1:p.Thr25375Arg
|
|
XM_011511730.1:c.50018C>G
(TTN)
|
XP_011510032.1:p.Thr16673Arg
|
|
XM_011511731.1:c.49877C>G
(TTN)
|
XP_011510033.1:p.Thr16626Arg
|
|
XM_017004819.1:c.75920C>G
(TTN)
|
XP_016860308.1:p.Thr25307Arg
|
|
XM_017004820.1:c.71318C>G
(TTN)
|
XP_016860309.1:p.Thr23773Arg
|
|
XM_017004821.1:c.71315C>G
(TTN)
|
XP_016860310.1:p.Thr23772Arg
|
|
XM_017004822.1:c.68357C>G
(TTN)
|
XP_016860311.1:p.Thr22786Arg
|
|
XM_017004823.1:c.49973C>G
(TTN)
|
XP_016860312.1:p.Thr16658Arg
|
|
XM_024453094.1:c.71468C>G
(TTN)
|
XP_024308862.1:p.Thr23823Arg
|
|
XM_024453095.1:c.71465C>G
(TTN)
|
XP_024308863.1:p.Thr23822Arg
|
|
XM_024453096.1:c.70898C>G
(TTN)
|
XP_024308864.1:p.Thr23633Arg
|
|
XM_024453097.1:c.68240C>G
(TTN)
|
XP_024308865.1:p.Thr22747Arg
|
|
XM_024453098.1:c.68159C>G
(TTN)
|
XP_024308866.1:p.Thr22720Arg
|
|
XM_024453099.1:c.49922C>G
(TTN)
|
XP_024308867.1:p.Thr16641Arg
|
|
XM_024453100.1:c.39776C>G
(TTN)
|
XP_024308868.1:p.Thr13259Arg
|
|