ENST00000342992.11:c.92882G>A
(TTN)
|
ENSP00000343764.6:p.Trp30961Ter
|
|
ENST00000342175.11:c.73967G>A
(TTN)
|
ENSP00000340554.6:p.Trp24656Ter
|
|
ENST00000359218.10:c.73766G>A
(TTN)
|
ENSP00000352154.5:p.Trp24589Ter
|
|
ENST00000342175.10:c.73967G>A
(TTN)
|
ENSP00000340554.6:p.Trp24656Ter
|
|
ENST00000342992.10:c.92882G>A
(TTN)
|
ENSP00000343764.6:p.Trp30961Ter
|
|
ENST00000359218.9:c.73766G>A
(TTN)
|
ENSP00000352154.5:p.Trp24589Ter
|
|
ENST00000460472.6:c.73391G>A
(TTN)
|
ENSP00000434586.1:p.Trp24464Ter
|
|
ENST00000589042.5:c.100586G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Trp33529Ter
|
|
ENST00000591111.5:c.95663G>A
(TTN)
|
ENSP00000465570.1:p.Trp31888Ter
|
|
ENST00000615779.4:c.95663G>A
(TTN)
|
ENSP00000483597.1:p.Trp31888Ter
|
|
NM_001256850.1:c.95663G>A
(TTN)
|
NP_001243779.1:p.Trp31888Ter
|
|
NM_001267550.2:c.100586G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Trp33529Ter
|
|
NM_003319.4:c.73391G>A
(TTN)
|
NP_003310.4:p.Trp24464Ter
|
|
NM_133378.4:c.92882G>A
(TTN)
|
NP_596869.4:p.Trp30961Ter
|
|
NM_133432.3:c.73766G>A
(TTN)
|
NP_597676.3:p.Trp24589Ter
|
|
NM_133437.4:c.73967G>A
(TTN)
|
NP_597681.4:p.Trp24656Ter
|
|
NR_038271.1:n.446+12525C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.316+333C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.99683G>A
(TTN)
|
XP_011510031.1:p.Trp33228Ter
|
|
XM_011511730.1:c.73577G>A
(TTN)
|
XP_011510032.1:p.Trp24526Ter
|
|
XM_011511731.1:c.73436G>A
(TTN)
|
XP_011510033.1:p.Trp24479Ter
|
|
XM_017004819.1:c.99479G>A
(TTN)
|
XP_016860308.1:p.Trp33160Ter
|
|
XM_017004820.1:c.94877G>A
(TTN)
|
XP_016860309.1:p.Trp31626Ter
|
|
XM_017004821.1:c.94874G>A
(TTN)
|
XP_016860310.1:p.Trp31625Ter
|
|
XM_017004822.1:c.91916G>A
(TTN)
|
XP_016860311.1:p.Trp30639Ter
|
|
XM_017004823.1:c.73532G>A
(TTN)
|
XP_016860312.1:p.Trp24511Ter
|
|
XM_024453094.1:c.95027G>A
(TTN)
|
XP_024308862.1:p.Trp31676Ter
|
|
XM_024453095.1:c.95024G>A
(TTN)
|
XP_024308863.1:p.Trp31675Ter
|
|
XM_024453096.1:c.94457G>A
(TTN)
|
XP_024308864.1:p.Trp31486Ter
|
|
XM_024453097.1:c.91799G>A
(TTN)
|
XP_024308865.1:p.Trp30600Ter
|
|
XM_024453098.1:c.91718G>A
(TTN)
|
XP_024308866.1:p.Trp30573Ter
|
|
XM_024453099.1:c.73481G>A
(TTN)
|
XP_024308867.1:p.Trp24494Ter
|
|
XM_024453100.1:c.63335G>A
(TTN)
|
XP_024308868.1:p.Trp21112Ter
|
|