ENST00000342992.11:c.79839T>C
(TTN)
|
ENSP00000343764.6:p.Ser26613=
|
|
ENST00000342175.11:c.60924T>C
(TTN)
|
ENSP00000340554.6:p.Ser20308=
|
|
ENST00000359218.10:c.60723T>C
(TTN)
|
ENSP00000352154.5:p.Ser20241=
|
|
ENST00000342175.10:c.60924T>C
(TTN)
|
ENSP00000340554.6:p.Ser20308=
|
|
ENST00000342992.10:c.79839T>C
(TTN)
|
ENSP00000343764.6:p.Ser26613=
|
|
ENST00000359218.9:c.60723T>C
(TTN)
|
ENSP00000352154.5:p.Ser20241=
|
|
ENST00000460472.6:c.60348T>C
(TTN)
|
ENSP00000434586.1:p.Ser20116=
|
|
ENST00000589042.5:c.87543T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser29181=
|
|
ENST00000591111.5:c.82620T>C
(TTN)
|
ENSP00000465570.1:p.Ser27540=
|
|
ENST00000615779.4:c.82620T>C
(TTN)
|
ENSP00000483597.1:p.Ser27540=
|
|
NM_001256850.1:c.82620T>C
(TTN)
|
NP_001243779.1:p.Ser27540=
|
|
NM_001267550.2:c.87543T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ser29181=
|
|
NM_003319.4:c.60348T>C
(TTN)
|
NP_003310.4:p.Ser20116=
|
|
NM_133378.4:c.79839T>C
(TTN)
|
NP_596869.4:p.Ser26613=
|
|
NM_133432.3:c.60723T>C
(TTN)
|
NP_597676.3:p.Ser20241=
|
|
NM_133437.4:c.60924T>C
(TTN)
|
NP_597681.4:p.Ser20308=
|
|
NR_038271.1:n.447-13489A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+15450A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.86640T>C
(TTN)
|
XP_011510031.1:p.Ser28880=
|
|
XM_011511730.1:c.60534T>C
(TTN)
|
XP_011510032.1:p.Ser20178=
|
|
XM_011511731.1:c.60393T>C
(TTN)
|
XP_011510033.1:p.Ser20131=
|
|
XM_017004819.1:c.86436T>C
(TTN)
|
XP_016860308.1:p.Ser28812=
|
|
XM_017004820.1:c.81834T>C
(TTN)
|
XP_016860309.1:p.Ser27278=
|
|
XM_017004821.1:c.81831T>C
(TTN)
|
XP_016860310.1:p.Ser27277=
|
|
XM_017004822.1:c.78873T>C
(TTN)
|
XP_016860311.1:p.Ser26291=
|
|
XM_017004823.1:c.60489T>C
(TTN)
|
XP_016860312.1:p.Ser20163=
|
|
XM_024453094.1:c.81984T>C
(TTN)
|
XP_024308862.1:p.Ser27328=
|
|
XM_024453095.1:c.81981T>C
(TTN)
|
XP_024308863.1:p.Ser27327=
|
|
XM_024453096.1:c.81414T>C
(TTN)
|
XP_024308864.1:p.Ser27138=
|
|
XM_024453097.1:c.78756T>C
(TTN)
|
XP_024308865.1:p.Ser26252=
|
|
XM_024453098.1:c.78675T>C
(TTN)
|
XP_024308866.1:p.Ser26225=
|
|
XM_024453099.1:c.60438T>C
(TTN)
|
XP_024308867.1:p.Ser20146=
|
|
XM_024453100.1:c.50292T>C
(TTN)
|
XP_024308868.1:p.Ser16764=
|
|