ENST00000342992.11:c.67969G>A
(TTN)
|
ENSP00000343764.6:p.Ala22657Thr
|
|
ENST00000342175.11:c.49054G>A
(TTN)
|
ENSP00000340554.6:p.Ala16352Thr
|
|
ENST00000359218.10:c.48853G>A
(TTN)
|
ENSP00000352154.5:p.Ala16285Thr
|
|
ENST00000342175.10:c.49054G>A
(TTN)
|
ENSP00000340554.6:p.Ala16352Thr
|
|
ENST00000342992.10:c.67969G>A
(TTN)
|
ENSP00000343764.6:p.Ala22657Thr
|
|
ENST00000359218.9:c.48853G>A
(TTN)
|
ENSP00000352154.5:p.Ala16285Thr
|
|
ENST00000460472.6:c.48478G>A
(TTN)
|
ENSP00000434586.1:p.Ala16160Thr
|
|
ENST00000589042.5:c.75673G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala25225Thr
|
|
ENST00000591111.5:c.70750G>A
(TTN)
|
ENSP00000465570.1:p.Ala23584Thr
|
|
ENST00000615779.4:c.70750G>A
(TTN)
|
ENSP00000483597.1:p.Ala23584Thr
|
|
NM_001256850.1:c.70750G>A
(TTN)
|
NP_001243779.1:p.Ala23584Thr
|
|
NM_001267550.2:c.75673G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala25225Thr
|
|
NM_003319.4:c.48478G>A
(TTN)
|
NP_003310.4:p.Ala16160Thr
|
|
NM_133378.4:c.67969G>A
(TTN)
|
NP_596869.4:p.Ala22657Thr
|
|
NM_133432.3:c.48853G>A
(TTN)
|
NP_597676.3:p.Ala16285Thr
|
|
NM_133437.4:c.49054G>A
(TTN)
|
NP_597681.4:p.Ala16352Thr
|
|
NR_038271.1:n.447-841C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12113C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.74770G>A
(TTN)
|
XP_011510031.1:p.Ala24924Thr
|
|
XM_011511730.1:c.48664G>A
(TTN)
|
XP_011510032.1:p.Ala16222Thr
|
|
XM_011511731.1:c.48523G>A
(TTN)
|
XP_011510033.1:p.Ala16175Thr
|
|
XM_017004819.1:c.74566G>A
(TTN)
|
XP_016860308.1:p.Ala24856Thr
|
|
XM_017004820.1:c.69964G>A
(TTN)
|
XP_016860309.1:p.Ala23322Thr
|
|
XM_017004821.1:c.69961G>A
(TTN)
|
XP_016860310.1:p.Ala23321Thr
|
|
XM_017004822.1:c.67003G>A
(TTN)
|
XP_016860311.1:p.Ala22335Thr
|
|
XM_017004823.1:c.48619G>A
(TTN)
|
XP_016860312.1:p.Ala16207Thr
|
|
XM_024453094.1:c.70114G>A
(TTN)
|
XP_024308862.1:p.Ala23372Thr
|
|
XM_024453095.1:c.70111G>A
(TTN)
|
XP_024308863.1:p.Ala23371Thr
|
|
XM_024453096.1:c.69544G>A
(TTN)
|
XP_024308864.1:p.Ala23182Thr
|
|
XM_024453097.1:c.66886G>A
(TTN)
|
XP_024308865.1:p.Ala22296Thr
|
|
XM_024453098.1:c.66805G>A
(TTN)
|
XP_024308866.1:p.Ala22269Thr
|
|
XM_024453099.1:c.48568G>A
(TTN)
|
XP_024308867.1:p.Ala16190Thr
|
|
XM_024453100.1:c.38422G>A
(TTN)
|
XP_024308868.1:p.Ala12808Thr
|
|