ENST00000342992.11:c.86287G>T
(TTN)
|
ENSP00000343764.6:p.Gly28763Ter
|
|
ENST00000342175.11:c.67372G>T
(TTN)
|
ENSP00000340554.6:p.Gly22458Ter
|
|
ENST00000359218.10:c.67171G>T
(TTN)
|
ENSP00000352154.5:p.Gly22391Ter
|
|
ENST00000342175.10:c.67372G>T
(TTN)
|
ENSP00000340554.6:p.Gly22458Ter
|
|
ENST00000342992.10:c.86287G>T
(TTN)
|
ENSP00000343764.6:p.Gly28763Ter
|
|
ENST00000359218.9:c.67171G>T
(TTN)
|
ENSP00000352154.5:p.Gly22391Ter
|
|
ENST00000460472.6:c.66796G>T
(TTN)
|
ENSP00000434586.1:p.Gly22266Ter
|
|
ENST00000589042.5:c.93991G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly31331Ter
|
|
ENST00000591111.5:c.89068G>T
(TTN)
|
ENSP00000465570.1:p.Gly29690Ter
|
|
ENST00000615779.4:c.89068G>T
(TTN)
|
ENSP00000483597.1:p.Gly29690Ter
|
|
NM_001256850.1:c.89068G>T
(TTN)
|
NP_001243779.1:p.Gly29690Ter
|
|
NM_001267550.2:c.93991G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly31331Ter
|
|
NM_003319.4:c.66796G>T
(TTN)
|
NP_003310.4:p.Gly22266Ter
|
|
NM_133378.4:c.86287G>T
(TTN)
|
NP_596869.4:p.Gly28763Ter
|
|
NM_133432.3:c.67171G>T
(TTN)
|
NP_597676.3:p.Gly22391Ter
|
|
NM_133437.4:c.67372G>T
(TTN)
|
NP_597681.4:p.Gly22458Ter
|
|
NR_038271.1:n.447-23665C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+5274C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.93088G>T
(TTN)
|
XP_011510031.1:p.Gly31030Ter
|
|
XM_011511730.1:c.66982G>T
(TTN)
|
XP_011510032.1:p.Gly22328Ter
|
|
XM_011511731.1:c.66841G>T
(TTN)
|
XP_011510033.1:p.Gly22281Ter
|
|
XM_017004819.1:c.92884G>T
(TTN)
|
XP_016860308.1:p.Gly30962Ter
|
|
XM_017004820.1:c.88282G>T
(TTN)
|
XP_016860309.1:p.Gly29428Ter
|
|
XM_017004821.1:c.88279G>T
(TTN)
|
XP_016860310.1:p.Gly29427Ter
|
|
XM_017004822.1:c.85321G>T
(TTN)
|
XP_016860311.1:p.Gly28441Ter
|
|
XM_017004823.1:c.66937G>T
(TTN)
|
XP_016860312.1:p.Gly22313Ter
|
|
XM_024453094.1:c.88432G>T
(TTN)
|
XP_024308862.1:p.Gly29478Ter
|
|
XM_024453095.1:c.88429G>T
(TTN)
|
XP_024308863.1:p.Gly29477Ter
|
|
XM_024453096.1:c.87862G>T
(TTN)
|
XP_024308864.1:p.Gly29288Ter
|
|
XM_024453097.1:c.85204G>T
(TTN)
|
XP_024308865.1:p.Gly28402Ter
|
|
XM_024453098.1:c.85123G>T
(TTN)
|
XP_024308866.1:p.Gly28375Ter
|
|
XM_024453099.1:c.66886G>T
(TTN)
|
XP_024308867.1:p.Gly22296Ter
|
|
XM_024453100.1:c.56740G>T
(TTN)
|
XP_024308868.1:p.Gly18914Ter
|
|