ENST00000342992.11:c.83358A>T
(TTN)
|
ENSP00000343764.6:p.Ser27786=
|
|
ENST00000342175.11:c.64443A>T
(TTN)
|
ENSP00000340554.6:p.Ser21481=
|
|
ENST00000359218.10:c.64242A>T
(TTN)
|
ENSP00000352154.5:p.Ser21414=
|
|
ENST00000342175.10:c.64443A>T
(TTN)
|
ENSP00000340554.6:p.Ser21481=
|
|
ENST00000342992.10:c.83358A>T
(TTN)
|
ENSP00000343764.6:p.Ser27786=
|
|
ENST00000359218.9:c.64242A>T
(TTN)
|
ENSP00000352154.5:p.Ser21414=
|
|
ENST00000460472.6:c.63867A>T
(TTN)
|
ENSP00000434586.1:p.Ser21289=
|
|
ENST00000589042.5:c.91062A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser30354=
|
|
ENST00000591111.5:c.86139A>T
(TTN)
|
ENSP00000465570.1:p.Ser28713=
|
|
ENST00000615779.4:c.86139A>T
(TTN)
|
ENSP00000483597.1:p.Ser28713=
|
|
NM_001256850.1:c.86139A>T
(TTN)
|
NP_001243779.1:p.Ser28713=
|
|
NM_001267550.2:c.91062A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ser30354=
|
|
NM_003319.4:c.63867A>T
(TTN)
|
NP_003310.4:p.Ser21289=
|
|
NM_133378.4:c.83358A>T
(TTN)
|
NP_596869.4:p.Ser27786=
|
|
NM_133432.3:c.64242A>T
(TTN)
|
NP_597676.3:p.Ser21414=
|
|
NM_133437.4:c.64443A>T
(TTN)
|
NP_597681.4:p.Ser21481=
|
|
NR_038271.1:n.447-19462T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9477T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.90159A>T
(TTN)
|
XP_011510031.1:p.Ser30053=
|
|
XM_011511730.1:c.64053A>T
(TTN)
|
XP_011510032.1:p.Ser21351=
|
|
XM_011511731.1:c.63912A>T
(TTN)
|
XP_011510033.1:p.Ser21304=
|
|
XM_017004819.1:c.89955A>T
(TTN)
|
XP_016860308.1:p.Ser29985=
|
|
XM_017004820.1:c.85353A>T
(TTN)
|
XP_016860309.1:p.Ser28451=
|
|
XM_017004821.1:c.85350A>T
(TTN)
|
XP_016860310.1:p.Ser28450=
|
|
XM_017004822.1:c.82392A>T
(TTN)
|
XP_016860311.1:p.Ser27464=
|
|
XM_017004823.1:c.64008A>T
(TTN)
|
XP_016860312.1:p.Ser21336=
|
|
XM_024453094.1:c.85503A>T
(TTN)
|
XP_024308862.1:p.Ser28501=
|
|
XM_024453095.1:c.85500A>T
(TTN)
|
XP_024308863.1:p.Ser28500=
|
|
XM_024453096.1:c.84933A>T
(TTN)
|
XP_024308864.1:p.Ser28311=
|
|
XM_024453097.1:c.82275A>T
(TTN)
|
XP_024308865.1:p.Ser27425=
|
|
XM_024453098.1:c.82194A>T
(TTN)
|
XP_024308866.1:p.Ser27398=
|
|
XM_024453099.1:c.63957A>T
(TTN)
|
XP_024308867.1:p.Ser21319=
|
|
XM_024453100.1:c.53811A>T
(TTN)
|
XP_024308868.1:p.Ser17937=
|
|