ENST00000342992.11:c.87011C>T
(TTN)
|
ENSP00000343764.6:p.Thr29004Ile
|
|
ENST00000342175.11:c.68096C>T
(TTN)
|
ENSP00000340554.6:p.Thr22699Ile
|
|
ENST00000359218.10:c.67895C>T
(TTN)
|
ENSP00000352154.5:p.Thr22632Ile
|
|
ENST00000342175.10:c.68096C>T
(TTN)
|
ENSP00000340554.6:p.Thr22699Ile
|
|
ENST00000342992.10:c.87011C>T
(TTN)
|
ENSP00000343764.6:p.Thr29004Ile
|
|
ENST00000359218.9:c.67895C>T
(TTN)
|
ENSP00000352154.5:p.Thr22632Ile
|
|
ENST00000460472.6:c.67520C>T
(TTN)
|
ENSP00000434586.1:p.Thr22507Ile
|
|
ENST00000589042.5:c.94715C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31572Ile
|
|
ENST00000591111.5:c.89792C>T
(TTN)
|
ENSP00000465570.1:p.Thr29931Ile
|
|
ENST00000615779.4:c.89792C>T
(TTN)
|
ENSP00000483597.1:p.Thr29931Ile
|
|
NM_001256850.1:c.89792C>T
(TTN)
|
NP_001243779.1:p.Thr29931Ile
|
|
NM_001267550.2:c.94715C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31572Ile
|
|
NM_003319.4:c.67520C>T
(TTN)
|
NP_003310.4:p.Thr22507Ile
|
|
NM_133378.4:c.87011C>T
(TTN)
|
NP_596869.4:p.Thr29004Ile
|
|
NM_133432.3:c.67895C>T
(TTN)
|
NP_597676.3:p.Thr22632Ile
|
|
NM_133437.4:c.68096C>T
(TTN)
|
NP_597681.4:p.Thr22699Ile
|
|
NR_038271.1:n.446+23077G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+4352G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.93812C>T
(TTN)
|
XP_011510031.1:p.Thr31271Ile
|
|
XM_011511730.1:c.67706C>T
(TTN)
|
XP_011510032.1:p.Thr22569Ile
|
|
XM_011511731.1:c.67565C>T
(TTN)
|
XP_011510033.1:p.Thr22522Ile
|
|
XM_017004819.1:c.93608C>T
(TTN)
|
XP_016860308.1:p.Thr31203Ile
|
|
XM_017004820.1:c.89006C>T
(TTN)
|
XP_016860309.1:p.Thr29669Ile
|
|
XM_017004821.1:c.89003C>T
(TTN)
|
XP_016860310.1:p.Thr29668Ile
|
|
XM_017004822.1:c.86045C>T
(TTN)
|
XP_016860311.1:p.Thr28682Ile
|
|
XM_017004823.1:c.67661C>T
(TTN)
|
XP_016860312.1:p.Thr22554Ile
|
|
XM_024453094.1:c.89156C>T
(TTN)
|
XP_024308862.1:p.Thr29719Ile
|
|
XM_024453095.1:c.89153C>T
(TTN)
|
XP_024308863.1:p.Thr29718Ile
|
|
XM_024453096.1:c.88586C>T
(TTN)
|
XP_024308864.1:p.Thr29529Ile
|
|
XM_024453097.1:c.85928C>T
(TTN)
|
XP_024308865.1:p.Thr28643Ile
|
|
XM_024453098.1:c.85847C>T
(TTN)
|
XP_024308866.1:p.Thr28616Ile
|
|
XM_024453099.1:c.67610C>T
(TTN)
|
XP_024308867.1:p.Thr22537Ile
|
|
XM_024453100.1:c.57464C>T
(TTN)
|
XP_024308868.1:p.Thr19155Ile
|
|