ENST00000342992.11:c.52898G>T
(TTN)
|
ENSP00000343764.6:p.Gly17633Val
|
|
ENST00000342175.11:c.33983G>T
(TTN)
|
ENSP00000340554.6:p.Gly11328Val
|
|
ENST00000359218.10:c.33782G>T
(TTN)
|
ENSP00000352154.5:p.Gly11261Val
|
|
ENST00000342175.10:c.33983G>T
(TTN)
|
ENSP00000340554.6:p.Gly11328Val
|
|
ENST00000342992.10:c.52898G>T
(TTN)
|
ENSP00000343764.6:p.Gly17633Val
|
|
ENST00000359218.9:c.33782G>T
(TTN)
|
ENSP00000352154.5:p.Gly11261Val
|
|
ENST00000460472.6:c.33407G>T
(TTN)
|
ENSP00000434586.1:p.Gly11136Val
|
|
ENST00000589042.5:c.60602G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly20201Val
|
|
ENST00000591111.5:c.55679G>T
(TTN)
|
ENSP00000465570.1:p.Gly18560Val
|
|
ENST00000615779.4:c.55679G>T
(TTN)
|
ENSP00000483597.1:p.Gly18560Val
|
|
NM_001256850.1:c.55679G>T
(TTN)
|
NP_001243779.1:p.Gly18560Val
|
|
NM_001267550.2:c.60602G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly20201Val
|
|
NM_003319.4:c.33407G>T
(TTN)
|
NP_003310.4:p.Gly11136Val
|
|
NM_133378.4:c.52898G>T
(TTN)
|
NP_596869.4:p.Gly17633Val
|
|
NM_133432.3:c.33782G>T
(TTN)
|
NP_597676.3:p.Gly11261Val
|
|
NM_133437.4:c.33983G>T
(TTN)
|
NP_597681.4:p.Gly11328Val
|
|
NR_038271.1:n.597-6473C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-16C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.59699G>T
(TTN)
|
XP_011510031.1:p.Gly19900Val
|
|
XM_011511730.1:c.33593G>T
(TTN)
|
XP_011510032.1:p.Gly11198Val
|
|
XM_011511731.1:c.33452G>T
(TTN)
|
XP_011510033.1:p.Gly11151Val
|
|
XM_017004819.1:c.59495G>T
(TTN)
|
XP_016860308.1:p.Gly19832Val
|
|
XM_017004820.1:c.54893G>T
(TTN)
|
XP_016860309.1:p.Gly18298Val
|
|
XM_017004821.1:c.54890G>T
(TTN)
|
XP_016860310.1:p.Gly18297Val
|
|
XM_017004822.1:c.51932G>T
(TTN)
|
XP_016860311.1:p.Gly17311Val
|
|
XM_017004823.1:c.33548G>T
(TTN)
|
XP_016860312.1:p.Gly11183Val
|
|
XM_024453094.1:c.55043G>T
(TTN)
|
XP_024308862.1:p.Gly18348Val
|
|
XM_024453095.1:c.55040G>T
(TTN)
|
XP_024308863.1:p.Gly18347Val
|
|
XM_024453096.1:c.54473G>T
(TTN)
|
XP_024308864.1:p.Gly18158Val
|
|
XM_024453097.1:c.51815G>T
(TTN)
|
XP_024308865.1:p.Gly17272Val
|
|
XM_024453098.1:c.51734G>T
(TTN)
|
XP_024308866.1:p.Gly17245Val
|
|
XM_024453099.1:c.33497G>T
(TTN)
|
XP_024308867.1:p.Gly11166Val
|
|
XM_024453100.1:c.23351G>T
(TTN)
|
XP_024308868.1:p.Gly7784Val
|
|