ENST00000342992.11:c.71223T>C
(TTN)
|
ENSP00000343764.6:p.Ser23741=
|
|
ENST00000342175.11:c.52308T>C
(TTN)
|
ENSP00000340554.6:p.Ser17436=
|
|
ENST00000359218.10:c.52107T>C
(TTN)
|
ENSP00000352154.5:p.Ser17369=
|
|
ENST00000342175.10:c.52308T>C
(TTN)
|
ENSP00000340554.6:p.Ser17436=
|
|
ENST00000342992.10:c.71223T>C
(TTN)
|
ENSP00000343764.6:p.Ser23741=
|
|
ENST00000359218.9:c.52107T>C
(TTN)
|
ENSP00000352154.5:p.Ser17369=
|
|
ENST00000460472.6:c.51732T>C
(TTN)
|
ENSP00000434586.1:p.Ser17244=
|
|
ENST00000589042.5:c.78927T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser26309=
|
|
ENST00000591111.5:c.74004T>C
(TTN)
|
ENSP00000465570.1:p.Ser24668=
|
|
ENST00000615779.4:c.74004T>C
(TTN)
|
ENSP00000483597.1:p.Ser24668=
|
|
NM_001256850.1:c.74004T>C
(TTN)
|
NP_001243779.1:p.Ser24668=
|
|
NM_001267550.2:c.78927T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ser26309=
|
|
NM_003319.4:c.51732T>C
(TTN)
|
NP_003310.4:p.Ser17244=
|
|
NM_133378.4:c.71223T>C
(TTN)
|
NP_596869.4:p.Ser23741=
|
|
NM_133432.3:c.52107T>C
(TTN)
|
NP_597676.3:p.Ser17369=
|
|
NM_133437.4:c.52308T>C
(TTN)
|
NP_597681.4:p.Ser17436=
|
|
NR_038271.1:n.447-4095A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-15367A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.78024T>C
(TTN)
|
XP_011510031.1:p.Ser26008=
|
|
XM_011511730.1:c.51918T>C
(TTN)
|
XP_011510032.1:p.Ser17306=
|
|
XM_011511731.1:c.51777T>C
(TTN)
|
XP_011510033.1:p.Ser17259=
|
|
XM_017004819.1:c.77820T>C
(TTN)
|
XP_016860308.1:p.Ser25940=
|
|
XM_017004820.1:c.73218T>C
(TTN)
|
XP_016860309.1:p.Ser24406=
|
|
XM_017004821.1:c.73215T>C
(TTN)
|
XP_016860310.1:p.Ser24405=
|
|
XM_017004822.1:c.70257T>C
(TTN)
|
XP_016860311.1:p.Ser23419=
|
|
XM_017004823.1:c.51873T>C
(TTN)
|
XP_016860312.1:p.Ser17291=
|
|
XM_024453094.1:c.73368T>C
(TTN)
|
XP_024308862.1:p.Ser24456=
|
|
XM_024453095.1:c.73365T>C
(TTN)
|
XP_024308863.1:p.Ser24455=
|
|
XM_024453096.1:c.72798T>C
(TTN)
|
XP_024308864.1:p.Ser24266=
|
|
XM_024453097.1:c.70140T>C
(TTN)
|
XP_024308865.1:p.Ser23380=
|
|
XM_024453098.1:c.70059T>C
(TTN)
|
XP_024308866.1:p.Ser23353=
|
|
XM_024453099.1:c.51822T>C
(TTN)
|
XP_024308867.1:p.Ser17274=
|
|
XM_024453100.1:c.41676T>C
(TTN)
|
XP_024308868.1:p.Ser13892=
|
|