ENST00000342992.11:c.47365G>T
(TTN)
|
ENSP00000343764.6:p.Glu15789Ter
|
|
ENST00000342175.11:c.28450G>T
(TTN)
|
ENSP00000340554.6:p.Glu9484Ter
|
|
ENST00000359218.10:c.28249G>T
(TTN)
|
ENSP00000352154.5:p.Glu9417Ter
|
|
ENST00000342175.10:c.28450G>T
(TTN)
|
ENSP00000340554.6:p.Glu9484Ter
|
|
ENST00000342992.10:c.47365G>T
(TTN)
|
ENSP00000343764.6:p.Glu15789Ter
|
|
ENST00000359218.9:c.28249G>T
(TTN)
|
ENSP00000352154.5:p.Glu9417Ter
|
|
ENST00000460472.6:c.27874G>T
(TTN)
|
ENSP00000434586.1:p.Glu9292Ter
|
|
ENST00000589042.5:c.55069G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu18357Ter
|
|
ENST00000591111.5:c.50146G>T
(TTN)
|
ENSP00000465570.1:p.Glu16716Ter
|
|
ENST00000615779.4:c.50146G>T
(TTN)
|
ENSP00000483597.1:p.Glu16716Ter
|
|
NM_001256850.1:c.50146G>T
(TTN)
|
NP_001243779.1:p.Glu16716Ter
|
|
NM_001267550.2:c.55069G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu18357Ter
|
|
NM_003319.4:c.27874G>T
(TTN)
|
NP_003310.4:p.Glu9292Ter
|
|
NM_133378.4:c.47365G>T
(TTN)
|
NP_596869.4:p.Glu15789Ter
|
|
NM_133432.3:c.28249G>T
(TTN)
|
NP_597676.3:p.Glu9417Ter
|
|
NM_133437.4:c.28450G>T
(TTN)
|
NP_597681.4:p.Glu9484Ter
|
|
NR_038271.1:n.682+4652C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+1666C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.54166G>T
(TTN)
|
XP_011510031.1:p.Glu18056Ter
|
|
XM_011511730.1:c.28060G>T
(TTN)
|
XP_011510032.1:p.Glu9354Ter
|
|
XM_011511731.1:c.27919G>T
(TTN)
|
XP_011510033.1:p.Glu9307Ter
|
|
XM_017004819.1:c.53962G>T
(TTN)
|
XP_016860308.1:p.Glu17988Ter
|
|
XM_017004820.1:c.49360G>T
(TTN)
|
XP_016860309.1:p.Glu16454Ter
|
|
XM_017004821.1:c.49357G>T
(TTN)
|
XP_016860310.1:p.Glu16453Ter
|
|
XM_017004822.1:c.46399G>T
(TTN)
|
XP_016860311.1:p.Glu15467Ter
|
|
XM_017004823.1:c.28015G>T
(TTN)
|
XP_016860312.1:p.Glu9339Ter
|
|
XM_024453094.1:c.49510G>T
(TTN)
|
XP_024308862.1:p.Glu16504Ter
|
|
XM_024453095.1:c.49507G>T
(TTN)
|
XP_024308863.1:p.Glu16503Ter
|
|
XM_024453096.1:c.48940G>T
(TTN)
|
XP_024308864.1:p.Glu16314Ter
|
|
XM_024453097.1:c.46282G>T
(TTN)
|
XP_024308865.1:p.Glu15428Ter
|
|
XM_024453098.1:c.46201G>T
(TTN)
|
XP_024308866.1:p.Glu15401Ter
|
|
XM_024453099.1:c.27964G>T
(TTN)
|
XP_024308867.1:p.Glu9322Ter
|
|
XM_024453100.1:c.17818G>T
(TTN)
|
XP_024308868.1:p.Glu5940Ter
|
|