ENST00000342992.11:c.71222C>T
(TTN)
|
ENSP00000343764.6:p.Ser23741Phe
|
|
ENST00000342175.11:c.52307C>T
(TTN)
|
ENSP00000340554.6:p.Ser17436Phe
|
|
ENST00000359218.10:c.52106C>T
(TTN)
|
ENSP00000352154.5:p.Ser17369Phe
|
|
ENST00000342175.10:c.52307C>T
(TTN)
|
ENSP00000340554.6:p.Ser17436Phe
|
|
ENST00000342992.10:c.71222C>T
(TTN)
|
ENSP00000343764.6:p.Ser23741Phe
|
|
ENST00000359218.9:c.52106C>T
(TTN)
|
ENSP00000352154.5:p.Ser17369Phe
|
|
ENST00000460472.6:c.51731C>T
(TTN)
|
ENSP00000434586.1:p.Ser17244Phe
|
|
ENST00000589042.5:c.78926C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser26309Phe
|
|
ENST00000591111.5:c.74003C>T
(TTN)
|
ENSP00000465570.1:p.Ser24668Phe
|
|
ENST00000615779.4:c.74003C>T
(TTN)
|
ENSP00000483597.1:p.Ser24668Phe
|
|
NM_001256850.1:c.74003C>T
(TTN)
|
NP_001243779.1:p.Ser24668Phe
|
|
NM_001267550.2:c.78926C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ser26309Phe
|
|
NM_003319.4:c.51731C>T
(TTN)
|
NP_003310.4:p.Ser17244Phe
|
|
NM_133378.4:c.71222C>T
(TTN)
|
NP_596869.4:p.Ser23741Phe
|
|
NM_133432.3:c.52106C>T
(TTN)
|
NP_597676.3:p.Ser17369Phe
|
|
NM_133437.4:c.52307C>T
(TTN)
|
NP_597681.4:p.Ser17436Phe
|
|
NR_038271.1:n.447-4094G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-15366G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.78023C>T
(TTN)
|
XP_011510031.1:p.Ser26008Phe
|
|
XM_011511730.1:c.51917C>T
(TTN)
|
XP_011510032.1:p.Ser17306Phe
|
|
XM_011511731.1:c.51776C>T
(TTN)
|
XP_011510033.1:p.Ser17259Phe
|
|
XM_017004819.1:c.77819C>T
(TTN)
|
XP_016860308.1:p.Ser25940Phe
|
|
XM_017004820.1:c.73217C>T
(TTN)
|
XP_016860309.1:p.Ser24406Phe
|
|
XM_017004821.1:c.73214C>T
(TTN)
|
XP_016860310.1:p.Ser24405Phe
|
|
XM_017004822.1:c.70256C>T
(TTN)
|
XP_016860311.1:p.Ser23419Phe
|
|
XM_017004823.1:c.51872C>T
(TTN)
|
XP_016860312.1:p.Ser17291Phe
|
|
XM_024453094.1:c.73367C>T
(TTN)
|
XP_024308862.1:p.Ser24456Phe
|
|
XM_024453095.1:c.73364C>T
(TTN)
|
XP_024308863.1:p.Ser24455Phe
|
|
XM_024453096.1:c.72797C>T
(TTN)
|
XP_024308864.1:p.Ser24266Phe
|
|
XM_024453097.1:c.70139C>T
(TTN)
|
XP_024308865.1:p.Ser23380Phe
|
|
XM_024453098.1:c.70058C>T
(TTN)
|
XP_024308866.1:p.Ser23353Phe
|
|
XM_024453099.1:c.51821C>T
(TTN)
|
XP_024308867.1:p.Ser17274Phe
|
|
XM_024453100.1:c.41675C>T
(TTN)
|
XP_024308868.1:p.Ser13892Phe
|
|