ENST00000342992.11:c.88155T>A
(TTN)
|
ENSP00000343764.6:p.Thr29385=
|
|
ENST00000342175.11:c.69240T>A
(TTN)
|
ENSP00000340554.6:p.Thr23080=
|
|
ENST00000359218.10:c.69039T>A
(TTN)
|
ENSP00000352154.5:p.Thr23013=
|
|
ENST00000342175.10:c.69240T>A
(TTN)
|
ENSP00000340554.6:p.Thr23080=
|
|
ENST00000342992.10:c.88155T>A
(TTN)
|
ENSP00000343764.6:p.Thr29385=
|
|
ENST00000359218.9:c.69039T>A
(TTN)
|
ENSP00000352154.5:p.Thr23013=
|
|
ENST00000460472.6:c.68664T>A
(TTN)
|
ENSP00000434586.1:p.Thr22888=
|
|
ENST00000589042.5:c.95859T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31953=
|
|
ENST00000591111.5:c.90936T>A
(TTN)
|
ENSP00000465570.1:p.Thr30312=
|
|
ENST00000615779.4:c.90936T>A
(TTN)
|
ENSP00000483597.1:p.Thr30312=
|
|
NM_001256850.1:c.90936T>A
(TTN)
|
NP_001243779.1:p.Thr30312=
|
|
NM_001267550.2:c.95859T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31953=
|
|
NM_003319.4:c.68664T>A
(TTN)
|
NP_003310.4:p.Thr22888=
|
|
NM_133378.4:c.88155T>A
(TTN)
|
NP_596869.4:p.Thr29385=
|
|
NM_133432.3:c.69039T>A
(TTN)
|
NP_597676.3:p.Thr23013=
|
|
NM_133437.4:c.69240T>A
(TTN)
|
NP_597681.4:p.Thr23080=
|
|
NR_038271.1:n.446+20734A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2009A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.94956T>A
(TTN)
|
XP_011510031.1:p.Thr31652=
|
|
XM_011511730.1:c.68850T>A
(TTN)
|
XP_011510032.1:p.Thr22950=
|
|
XM_011511731.1:c.68709T>A
(TTN)
|
XP_011510033.1:p.Thr22903=
|
|
XM_017004819.1:c.94752T>A
(TTN)
|
XP_016860308.1:p.Thr31584=
|
|
XM_017004820.1:c.90150T>A
(TTN)
|
XP_016860309.1:p.Thr30050=
|
|
XM_017004821.1:c.90147T>A
(TTN)
|
XP_016860310.1:p.Thr30049=
|
|
XM_017004822.1:c.87189T>A
(TTN)
|
XP_016860311.1:p.Thr29063=
|
|
XM_017004823.1:c.68805T>A
(TTN)
|
XP_016860312.1:p.Thr22935=
|
|
XM_024453094.1:c.90300T>A
(TTN)
|
XP_024308862.1:p.Thr30100=
|
|
XM_024453095.1:c.90297T>A
(TTN)
|
XP_024308863.1:p.Thr30099=
|
|
XM_024453096.1:c.89730T>A
(TTN)
|
XP_024308864.1:p.Thr29910=
|
|
XM_024453097.1:c.87072T>A
(TTN)
|
XP_024308865.1:p.Thr29024=
|
|
XM_024453098.1:c.86991T>A
(TTN)
|
XP_024308866.1:p.Thr28997=
|
|
XM_024453099.1:c.68754T>A
(TTN)
|
XP_024308867.1:p.Thr22918=
|
|
XM_024453100.1:c.58608T>A
(TTN)
|
XP_024308868.1:p.Thr19536=
|
|