ENST00000342992.11:c.60823+1G>T
(TTN)
|
ENSP00000343764.6:n.60823+1G>T
|
|
ENST00000342175.11:c.41908+1G>T
(TTN)
|
ENSP00000340554.6:n.41908+1G>T
|
|
ENST00000359218.10:c.41707+1G>T
(TTN)
|
ENSP00000352154.5:n.41707+1G>T
|
|
ENST00000342175.10:c.41908+1G>T
(TTN)
|
ENSP00000340554.6:n.41908+1G>T
|
|
ENST00000342992.10:c.60823+1G>T
(TTN)
|
ENSP00000343764.6:n.60823+1G>T
|
|
ENST00000359218.9:c.41707+1G>T
(TTN)
|
ENSP00000352154.5:n.41707+1G>T
|
|
ENST00000460472.6:c.41332+1G>T
(TTN)
|
ENSP00000434586.1:n.41332+1G>T
|
|
ENST00000589042.5:c.68527+1G>T
(TTN)
MANE Select
|
ENSP00000467141.1:n.68527+1G>T
|
|
ENST00000591111.5:c.63604+1G>T
(TTN)
|
ENSP00000465570.1:n.63604+1G>T
|
|
ENST00000615779.4:c.63604+1G>T
(TTN)
|
ENSP00000483597.1:n.63604+1G>T
|
|
NM_001256850.1:c.63604+1G>T
(TTN)
|
NP_001243779.1:n.63604+1G>T
|
|
NM_001267550.2:c.68527+1G>T
(TTN)
MANE Select
|
NP_001254479.2:n.68527+1G>T
|
|
NM_003319.4:c.41332+1G>T
(TTN)
|
NP_003310.4:n.41332+1G>T
|
|
NM_133378.4:c.60823+1G>T
(TTN)
|
NP_596869.4:n.60823+1G>T
|
|
NM_133432.3:c.41707+1G>T
(TTN)
|
NP_597676.3:n.41707+1G>T
|
|
NM_133437.4:c.41908+1G>T
(TTN)
|
NP_597681.4:n.41908+1G>T
|
|
NR_038271.1:n.596+6538C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-4585C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.67624+1G>T
(TTN)
|
XP_011510031.1:n.67624+1G>T
|
|
XM_011511730.1:c.41518+1G>T
(TTN)
|
XP_011510032.1:n.41518+1G>T
|
|
XM_011511731.1:c.41377+1G>T
(TTN)
|
XP_011510033.1:n.41377+1G>T
|
|
XM_017004819.1:c.67420+1G>T
(TTN)
|
XP_016860308.1:n.67420+1G>T
|
|
XM_017004820.1:c.62818+1G>T
(TTN)
|
XP_016860309.1:n.62818+1G>T
|
|
XM_017004821.1:c.62815+1G>T
(TTN)
|
XP_016860310.1:n.62815+1G>T
|
|
XM_017004822.1:c.59857+1G>T
(TTN)
|
XP_016860311.1:n.59857+1G>T
|
|
XM_017004823.1:c.41473+1G>T
(TTN)
|
XP_016860312.1:n.41473+1G>T
|
|
XM_024453094.1:c.62968+1G>T
(TTN)
|
XP_024308862.1:n.62968+1G>T
|
|
XM_024453095.1:c.62965+1G>T
(TTN)
|
XP_024308863.1:n.62965+1G>T
|
|
XM_024453096.1:c.62398+1G>T
(TTN)
|
XP_024308864.1:n.62398+1G>T
|
|
XM_024453097.1:c.59740+1G>T
(TTN)
|
XP_024308865.1:n.59740+1G>T
|
|
XM_024453098.1:c.59659+1G>T
(TTN)
|
XP_024308866.1:n.59659+1G>T
|
|
XM_024453099.1:c.41422+1G>T
(TTN)
|
XP_024308867.1:n.41422+1G>T
|
|
XM_024453100.1:c.31276+1G>T
(TTN)
|
XP_024308868.1:n.31276+1G>T
|
|