|
ENST00000342992.11:c.50566G>T
(TTN)
|
ENSP00000343764.6:p.Glu16856Ter
|
|
|
ENST00000342175.11:c.31651G>T
(TTN)
|
ENSP00000340554.6:p.Glu10551Ter
|
|
|
ENST00000359218.10:c.31450G>T
(TTN)
|
ENSP00000352154.5:p.Glu10484Ter
|
|
|
ENST00000342175.10:c.31651G>T
(TTN)
|
ENSP00000340554.6:p.Glu10551Ter
|
|
|
ENST00000342992.10:c.50566G>T
(TTN)
|
ENSP00000343764.6:p.Glu16856Ter
|
|
|
ENST00000359218.9:c.31450G>T
(TTN)
|
ENSP00000352154.5:p.Glu10484Ter
|
|
|
ENST00000460472.6:c.31075G>T
(TTN)
|
ENSP00000434586.1:p.Glu10359Ter
|
|
|
ENST00000589042.5:c.58270G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu19424Ter
|
|
|
ENST00000591111.5:c.53347G>T
(TTN)
|
ENSP00000465570.1:p.Glu17783Ter
|
|
|
ENST00000615779.4:c.53347G>T
(TTN)
|
ENSP00000483597.1:p.Glu17783Ter
|
|
|
NM_001256850.1:c.53347G>T
(TTN)
|
NP_001243779.1:p.Glu17783Ter
|
|
|
NM_001267550.2:c.58270G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu19424Ter
|
|
|
NM_003319.4:c.31075G>T
(TTN)
|
NP_003310.4:p.Glu10359Ter
|
|
|
NM_133378.4:c.50566G>T
(TTN)
|
NP_596869.4:p.Glu16856Ter
|
|
|
NM_133432.3:c.31450G>T
(TTN)
|
NP_597676.3:p.Glu10484Ter
|
|
|
NM_133437.4:c.31651G>T
(TTN)
|
NP_597681.4:p.Glu10551Ter
|
|
|
NR_038271.1:n.597-3473C>A
(TTN-AS1)
|
|
|
|
NR_038272.1:n.3364+2809C>A
(TTN-AS1)
|
|
|
|
XM_011511729.1:c.57367G>T
(TTN)
|
XP_011510031.1:p.Glu19123Ter
|
|
|
XM_011511730.1:c.31261G>T
(TTN)
|
XP_011510032.1:p.Glu10421Ter
|
|
|
XM_011511731.1:c.31120G>T
(TTN)
|
XP_011510033.1:p.Glu10374Ter
|
|
|
XM_017004819.1:c.57163G>T
(TTN)
|
XP_016860308.1:p.Glu19055Ter
|
|
|
XM_017004820.1:c.52561G>T
(TTN)
|
XP_016860309.1:p.Glu17521Ter
|
|
|
XM_017004821.1:c.52558G>T
(TTN)
|
XP_016860310.1:p.Glu17520Ter
|
|
|
XM_017004822.1:c.49600G>T
(TTN)
|
XP_016860311.1:p.Glu16534Ter
|
|
|
XM_017004823.1:c.31216G>T
(TTN)
|
XP_016860312.1:p.Glu10406Ter
|
|
|
XM_024453094.1:c.52711G>T
(TTN)
|
XP_024308862.1:p.Glu17571Ter
|
|
|
XM_024453095.1:c.52708G>T
(TTN)
|
XP_024308863.1:p.Glu17570Ter
|
|
|
XM_024453096.1:c.52141G>T
(TTN)
|
XP_024308864.1:p.Glu17381Ter
|
|
|
XM_024453097.1:c.49483G>T
(TTN)
|
XP_024308865.1:p.Glu16495Ter
|
|
|
XM_024453098.1:c.49402G>T
(TTN)
|
XP_024308866.1:p.Glu16468Ter
|
|
|
XM_024453099.1:c.31165G>T
(TTN)
|
XP_024308867.1:p.Glu10389Ter
|
|
|
XM_024453100.1:c.21019G>T
(TTN)
|
XP_024308868.1:p.Glu7007Ter
|
|
