ENST00000342992.11:c.69582T>C
(TTN)
|
ENSP00000343764.6:p.Thr23194=
|
|
ENST00000342175.11:c.50667T>C
(TTN)
|
ENSP00000340554.6:p.Thr16889=
|
|
ENST00000359218.10:c.50466T>C
(TTN)
|
ENSP00000352154.5:p.Thr16822=
|
|
ENST00000342175.10:c.50667T>C
(TTN)
|
ENSP00000340554.6:p.Thr16889=
|
|
ENST00000342992.10:c.69582T>C
(TTN)
|
ENSP00000343764.6:p.Thr23194=
|
|
ENST00000359218.9:c.50466T>C
(TTN)
|
ENSP00000352154.5:p.Thr16822=
|
|
ENST00000460472.6:c.50091T>C
(TTN)
|
ENSP00000434586.1:p.Thr16697=
|
|
ENST00000589042.5:c.77286T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr25762=
|
|
ENST00000591111.5:c.72363T>C
(TTN)
|
ENSP00000465570.1:p.Thr24121=
|
|
ENST00000615779.4:c.72363T>C
(TTN)
|
ENSP00000483597.1:p.Thr24121=
|
|
NM_001256850.1:c.72363T>C
(TTN)
|
NP_001243779.1:p.Thr24121=
|
|
NM_001267550.2:c.77286T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Thr25762=
|
|
NM_003319.4:c.50091T>C
(TTN)
|
NP_003310.4:p.Thr16697=
|
|
NM_133378.4:c.69582T>C
(TTN)
|
NP_596869.4:p.Thr23194=
|
|
NM_133432.3:c.50466T>C
(TTN)
|
NP_597676.3:p.Thr16822=
|
|
NM_133437.4:c.50667T>C
(TTN)
|
NP_597681.4:p.Thr16889=
|
|
NR_038271.1:n.447-2454A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13726A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.76383T>C
(TTN)
|
XP_011510031.1:p.Thr25461=
|
|
XM_011511730.1:c.50277T>C
(TTN)
|
XP_011510032.1:p.Thr16759=
|
|
XM_011511731.1:c.50136T>C
(TTN)
|
XP_011510033.1:p.Thr16712=
|
|
XM_017004819.1:c.76179T>C
(TTN)
|
XP_016860308.1:p.Thr25393=
|
|
XM_017004820.1:c.71577T>C
(TTN)
|
XP_016860309.1:p.Thr23859=
|
|
XM_017004821.1:c.71574T>C
(TTN)
|
XP_016860310.1:p.Thr23858=
|
|
XM_017004822.1:c.68616T>C
(TTN)
|
XP_016860311.1:p.Thr22872=
|
|
XM_017004823.1:c.50232T>C
(TTN)
|
XP_016860312.1:p.Thr16744=
|
|
XM_024453094.1:c.71727T>C
(TTN)
|
XP_024308862.1:p.Thr23909=
|
|
XM_024453095.1:c.71724T>C
(TTN)
|
XP_024308863.1:p.Thr23908=
|
|
XM_024453096.1:c.71157T>C
(TTN)
|
XP_024308864.1:p.Thr23719=
|
|
XM_024453097.1:c.68499T>C
(TTN)
|
XP_024308865.1:p.Thr22833=
|
|
XM_024453098.1:c.68418T>C
(TTN)
|
XP_024308866.1:p.Thr22806=
|
|
XM_024453099.1:c.50181T>C
(TTN)
|
XP_024308867.1:p.Thr16727=
|
|
XM_024453100.1:c.40035T>C
(TTN)
|
XP_024308868.1:p.Thr13345=
|
|