ENST00000342992.11:c.69429C>G
(TTN)
|
ENSP00000343764.6:p.Thr23143=
|
|
ENST00000342175.11:c.50514C>G
(TTN)
|
ENSP00000340554.6:p.Thr16838=
|
|
ENST00000359218.10:c.50313C>G
(TTN)
|
ENSP00000352154.5:p.Thr16771=
|
|
ENST00000342175.10:c.50514C>G
(TTN)
|
ENSP00000340554.6:p.Thr16838=
|
|
ENST00000342992.10:c.69429C>G
(TTN)
|
ENSP00000343764.6:p.Thr23143=
|
|
ENST00000359218.9:c.50313C>G
(TTN)
|
ENSP00000352154.5:p.Thr16771=
|
|
ENST00000460472.6:c.49938C>G
(TTN)
|
ENSP00000434586.1:p.Thr16646=
|
|
ENST00000589042.5:c.77133C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr25711=
|
|
ENST00000591111.5:c.72210C>G
(TTN)
|
ENSP00000465570.1:p.Thr24070=
|
|
ENST00000615779.4:c.72210C>G
(TTN)
|
ENSP00000483597.1:p.Thr24070=
|
|
NM_001256850.1:c.72210C>G
(TTN)
|
NP_001243779.1:p.Thr24070=
|
|
NM_001267550.2:c.77133C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr25711=
|
|
NM_003319.4:c.49938C>G
(TTN)
|
NP_003310.4:p.Thr16646=
|
|
NM_133378.4:c.69429C>G
(TTN)
|
NP_596869.4:p.Thr23143=
|
|
NM_133432.3:c.50313C>G
(TTN)
|
NP_597676.3:p.Thr16771=
|
|
NM_133437.4:c.50514C>G
(TTN)
|
NP_597681.4:p.Thr16838=
|
|
NR_038271.1:n.447-2301G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13573G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.76230C>G
(TTN)
|
XP_011510031.1:p.Thr25410=
|
|
XM_011511730.1:c.50124C>G
(TTN)
|
XP_011510032.1:p.Thr16708=
|
|
XM_011511731.1:c.49983C>G
(TTN)
|
XP_011510033.1:p.Thr16661=
|
|
XM_017004819.1:c.76026C>G
(TTN)
|
XP_016860308.1:p.Thr25342=
|
|
XM_017004820.1:c.71424C>G
(TTN)
|
XP_016860309.1:p.Thr23808=
|
|
XM_017004821.1:c.71421C>G
(TTN)
|
XP_016860310.1:p.Thr23807=
|
|
XM_017004822.1:c.68463C>G
(TTN)
|
XP_016860311.1:p.Thr22821=
|
|
XM_017004823.1:c.50079C>G
(TTN)
|
XP_016860312.1:p.Thr16693=
|
|
XM_024453094.1:c.71574C>G
(TTN)
|
XP_024308862.1:p.Thr23858=
|
|
XM_024453095.1:c.71571C>G
(TTN)
|
XP_024308863.1:p.Thr23857=
|
|
XM_024453096.1:c.71004C>G
(TTN)
|
XP_024308864.1:p.Thr23668=
|
|
XM_024453097.1:c.68346C>G
(TTN)
|
XP_024308865.1:p.Thr22782=
|
|
XM_024453098.1:c.68265C>G
(TTN)
|
XP_024308866.1:p.Thr22755=
|
|
XM_024453099.1:c.50028C>G
(TTN)
|
XP_024308867.1:p.Thr16676=
|
|
XM_024453100.1:c.39882C>G
(TTN)
|
XP_024308868.1:p.Thr13294=
|
|