ENST00000342992.11:c.67368T>A
(TTN)
|
ENSP00000343764.6:p.Thr22456=
|
|
ENST00000342175.11:c.48453T>A
(TTN)
|
ENSP00000340554.6:p.Thr16151=
|
|
ENST00000359218.10:c.48252T>A
(TTN)
|
ENSP00000352154.5:p.Thr16084=
|
|
ENST00000342175.10:c.48453T>A
(TTN)
|
ENSP00000340554.6:p.Thr16151=
|
|
ENST00000342992.10:c.67368T>A
(TTN)
|
ENSP00000343764.6:p.Thr22456=
|
|
ENST00000359218.9:c.48252T>A
(TTN)
|
ENSP00000352154.5:p.Thr16084=
|
|
ENST00000460472.6:c.47877T>A
(TTN)
|
ENSP00000434586.1:p.Thr15959=
|
|
ENST00000589042.5:c.75072T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr25024=
|
|
ENST00000591111.5:c.70149T>A
(TTN)
|
ENSP00000465570.1:p.Thr23383=
|
|
ENST00000615779.4:c.70149T>A
(TTN)
|
ENSP00000483597.1:p.Thr23383=
|
|
NM_001256850.1:c.70149T>A
(TTN)
|
NP_001243779.1:p.Thr23383=
|
|
NM_001267550.2:c.75072T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr25024=
|
|
NM_003319.4:c.47877T>A
(TTN)
|
NP_003310.4:p.Thr15959=
|
|
NM_133378.4:c.67368T>A
(TTN)
|
NP_596869.4:p.Thr22456=
|
|
NM_133432.3:c.48252T>A
(TTN)
|
NP_597676.3:p.Thr16084=
|
|
NM_133437.4:c.48453T>A
(TTN)
|
NP_597681.4:p.Thr16151=
|
|
NR_038271.1:n.447-240A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-11512A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.74169T>A
(TTN)
|
XP_011510031.1:p.Thr24723=
|
|
XM_011511730.1:c.48063T>A
(TTN)
|
XP_011510032.1:p.Thr16021=
|
|
XM_011511731.1:c.47922T>A
(TTN)
|
XP_011510033.1:p.Thr15974=
|
|
XM_017004819.1:c.73965T>A
(TTN)
|
XP_016860308.1:p.Thr24655=
|
|
XM_017004820.1:c.69363T>A
(TTN)
|
XP_016860309.1:p.Thr23121=
|
|
XM_017004821.1:c.69360T>A
(TTN)
|
XP_016860310.1:p.Thr23120=
|
|
XM_017004822.1:c.66402T>A
(TTN)
|
XP_016860311.1:p.Thr22134=
|
|
XM_017004823.1:c.48018T>A
(TTN)
|
XP_016860312.1:p.Thr16006=
|
|
XM_024453094.1:c.69513T>A
(TTN)
|
XP_024308862.1:p.Thr23171=
|
|
XM_024453095.1:c.69510T>A
(TTN)
|
XP_024308863.1:p.Thr23170=
|
|
XM_024453096.1:c.68943T>A
(TTN)
|
XP_024308864.1:p.Thr22981=
|
|
XM_024453097.1:c.66285T>A
(TTN)
|
XP_024308865.1:p.Thr22095=
|
|
XM_024453098.1:c.66204T>A
(TTN)
|
XP_024308866.1:p.Thr22068=
|
|
XM_024453099.1:c.47967T>A
(TTN)
|
XP_024308867.1:p.Thr15989=
|
|
XM_024453100.1:c.37821T>A
(TTN)
|
XP_024308868.1:p.Thr12607=
|
|