ENST00000342992.11:c.78792T>A
(TTN)
|
ENSP00000343764.6:p.Ser26264Arg
|
|
ENST00000342175.11:c.59877T>A
(TTN)
|
ENSP00000340554.6:p.Ser19959Arg
|
|
ENST00000359218.10:c.59676T>A
(TTN)
|
ENSP00000352154.5:p.Ser19892Arg
|
|
ENST00000342175.10:c.59877T>A
(TTN)
|
ENSP00000340554.6:p.Ser19959Arg
|
|
ENST00000342992.10:c.78792T>A
(TTN)
|
ENSP00000343764.6:p.Ser26264Arg
|
|
ENST00000359218.9:c.59676T>A
(TTN)
|
ENSP00000352154.5:p.Ser19892Arg
|
|
ENST00000460472.6:c.59301T>A
(TTN)
|
ENSP00000434586.1:p.Ser19767Arg
|
|
ENST00000589042.5:c.86496T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser28832Arg
|
|
ENST00000591111.5:c.81573T>A
(TTN)
|
ENSP00000465570.1:p.Ser27191Arg
|
|
ENST00000615779.4:c.81573T>A
(TTN)
|
ENSP00000483597.1:p.Ser27191Arg
|
|
NM_001256850.1:c.81573T>A
(TTN)
|
NP_001243779.1:p.Ser27191Arg
|
|
NM_001267550.2:c.86496T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser28832Arg
|
|
NM_003319.4:c.59301T>A
(TTN)
|
NP_003310.4:p.Ser19767Arg
|
|
NM_133378.4:c.78792T>A
(TTN)
|
NP_596869.4:p.Ser26264Arg
|
|
NM_133432.3:c.59676T>A
(TTN)
|
NP_597676.3:p.Ser19892Arg
|
|
NM_133437.4:c.59877T>A
(TTN)
|
NP_597681.4:p.Ser19959Arg
|
|
NR_038271.1:n.447-11664A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17275A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.85593T>A
(TTN)
|
XP_011510031.1:p.Ser28531Arg
|
|
XM_011511730.1:c.59487T>A
(TTN)
|
XP_011510032.1:p.Ser19829Arg
|
|
XM_011511731.1:c.59346T>A
(TTN)
|
XP_011510033.1:p.Ser19782Arg
|
|
XM_017004819.1:c.85389T>A
(TTN)
|
XP_016860308.1:p.Ser28463Arg
|
|
XM_017004820.1:c.80787T>A
(TTN)
|
XP_016860309.1:p.Ser26929Arg
|
|
XM_017004821.1:c.80784T>A
(TTN)
|
XP_016860310.1:p.Ser26928Arg
|
|
XM_017004822.1:c.77826T>A
(TTN)
|
XP_016860311.1:p.Ser25942Arg
|
|
XM_017004823.1:c.59442T>A
(TTN)
|
XP_016860312.1:p.Ser19814Arg
|
|
XM_024453094.1:c.80937T>A
(TTN)
|
XP_024308862.1:p.Ser26979Arg
|
|
XM_024453095.1:c.80934T>A
(TTN)
|
XP_024308863.1:p.Ser26978Arg
|
|
XM_024453096.1:c.80367T>A
(TTN)
|
XP_024308864.1:p.Ser26789Arg
|
|
XM_024453097.1:c.77709T>A
(TTN)
|
XP_024308865.1:p.Ser25903Arg
|
|
XM_024453098.1:c.77628T>A
(TTN)
|
XP_024308866.1:p.Ser25876Arg
|
|
XM_024453099.1:c.59391T>A
(TTN)
|
XP_024308867.1:p.Ser19797Arg
|
|
XM_024453100.1:c.49245T>A
(TTN)
|
XP_024308868.1:p.Ser16415Arg
|
|