ENST00000342992.11:c.84238G>A
(TTN)
|
ENSP00000343764.6:p.Gly28080Ser
|
|
ENST00000342175.11:c.65323G>A
(TTN)
|
ENSP00000340554.6:p.Gly21775Ser
|
|
ENST00000359218.10:c.65122G>A
(TTN)
|
ENSP00000352154.5:p.Gly21708Ser
|
|
ENST00000342175.10:c.65323G>A
(TTN)
|
ENSP00000340554.6:p.Gly21775Ser
|
|
ENST00000342992.10:c.84238G>A
(TTN)
|
ENSP00000343764.6:p.Gly28080Ser
|
|
ENST00000359218.9:c.65122G>A
(TTN)
|
ENSP00000352154.5:p.Gly21708Ser
|
|
ENST00000460472.6:c.64747G>A
(TTN)
|
ENSP00000434586.1:p.Gly21583Ser
|
|
ENST00000589042.5:c.91942G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly30648Ser
|
|
ENST00000591111.5:c.87019G>A
(TTN)
|
ENSP00000465570.1:p.Gly29007Ser
|
|
ENST00000615779.4:c.87019G>A
(TTN)
|
ENSP00000483597.1:p.Gly29007Ser
|
|
NM_001256850.1:c.87019G>A
(TTN)
|
NP_001243779.1:p.Gly29007Ser
|
|
NM_001267550.2:c.91942G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly30648Ser
|
|
NM_003319.4:c.64747G>A
(TTN)
|
NP_003310.4:p.Gly21583Ser
|
|
NM_133378.4:c.84238G>A
(TTN)
|
NP_596869.4:p.Gly28080Ser
|
|
NM_133432.3:c.65122G>A
(TTN)
|
NP_597676.3:p.Gly21708Ser
|
|
NM_133437.4:c.65323G>A
(TTN)
|
NP_597681.4:p.Gly21775Ser
|
|
NR_038271.1:n.447-21520C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+7419C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.91039G>A
(TTN)
|
XP_011510031.1:p.Gly30347Ser
|
|
XM_011511730.1:c.64933G>A
(TTN)
|
XP_011510032.1:p.Gly21645Ser
|
|
XM_011511731.1:c.64792G>A
(TTN)
|
XP_011510033.1:p.Gly21598Ser
|
|
XM_017004819.1:c.90835G>A
(TTN)
|
XP_016860308.1:p.Gly30279Ser
|
|
XM_017004820.1:c.86233G>A
(TTN)
|
XP_016860309.1:p.Gly28745Ser
|
|
XM_017004821.1:c.86230G>A
(TTN)
|
XP_016860310.1:p.Gly28744Ser
|
|
XM_017004822.1:c.83272G>A
(TTN)
|
XP_016860311.1:p.Gly27758Ser
|
|
XM_017004823.1:c.64888G>A
(TTN)
|
XP_016860312.1:p.Gly21630Ser
|
|
XM_024453094.1:c.86383G>A
(TTN)
|
XP_024308862.1:p.Gly28795Ser
|
|
XM_024453095.1:c.86380G>A
(TTN)
|
XP_024308863.1:p.Gly28794Ser
|
|
XM_024453096.1:c.85813G>A
(TTN)
|
XP_024308864.1:p.Gly28605Ser
|
|
XM_024453097.1:c.83155G>A
(TTN)
|
XP_024308865.1:p.Gly27719Ser
|
|
XM_024453098.1:c.83074G>A
(TTN)
|
XP_024308866.1:p.Gly27692Ser
|
|
XM_024453099.1:c.64837G>A
(TTN)
|
XP_024308867.1:p.Gly21613Ser
|
|
XM_024453100.1:c.54691G>A
(TTN)
|
XP_024308868.1:p.Gly18231Ser
|
|