ENST00000342992.11:c.98706A>G
(TTN)
|
ENSP00000343764.6:p.Glu32902=
|
|
ENST00000342175.11:c.79791A>G
(TTN)
|
ENSP00000340554.6:p.Glu26597=
|
|
ENST00000359218.10:c.79590A>G
(TTN)
|
ENSP00000352154.5:p.Glu26530=
|
|
ENST00000342175.10:c.79791A>G
(TTN)
|
ENSP00000340554.6:p.Glu26597=
|
|
ENST00000342992.10:c.98706A>G
(TTN)
|
ENSP00000343764.6:p.Glu32902=
|
|
ENST00000359218.9:c.79590A>G
(TTN)
|
ENSP00000352154.5:p.Glu26530=
|
|
ENST00000460472.6:c.79215A>G
(TTN)
|
ENSP00000434586.1:p.Glu26405=
|
|
ENST00000589042.5:c.106410A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35470=
|
|
ENST00000591111.5:c.101487A>G
(TTN)
|
ENSP00000465570.1:p.Glu33829=
|
|
ENST00000615779.4:c.101487A>G
(TTN)
|
ENSP00000483597.1:p.Glu33829=
|
|
NM_001256850.1:c.101487A>G
(TTN)
|
NP_001243779.1:p.Glu33829=
|
|
NM_001267550.2:c.106410A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35470=
|
|
NM_003319.4:c.79215A>G
(TTN)
|
NP_003310.4:p.Glu26405=
|
|
NM_133378.4:c.98706A>G
(TTN)
|
NP_596869.4:p.Glu32902=
|
|
NM_133432.3:c.79590A>G
(TTN)
|
NP_597676.3:p.Glu26530=
|
|
NM_133437.4:c.79791A>G
(TTN)
|
NP_597681.4:p.Glu26597=
|
|
NR_038271.1:n.446+6445T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5651T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105507A>G
(TTN)
|
XP_011510031.1:p.Glu35169=
|
|
XM_011511730.1:c.79401A>G
(TTN)
|
XP_011510032.1:p.Glu26467=
|
|
XM_011511731.1:c.79260A>G
(TTN)
|
XP_011510033.1:p.Glu26420=
|
|
XM_017004819.1:c.105303A>G
(TTN)
|
XP_016860308.1:p.Glu35101=
|
|
XM_017004820.1:c.100701A>G
(TTN)
|
XP_016860309.1:p.Glu33567=
|
|
XM_017004821.1:c.100698A>G
(TTN)
|
XP_016860310.1:p.Glu33566=
|
|
XM_017004822.1:c.97740A>G
(TTN)
|
XP_016860311.1:p.Glu32580=
|
|
XM_017004823.1:c.79356A>G
(TTN)
|
XP_016860312.1:p.Glu26452=
|
|
XM_024453094.1:c.100851A>G
(TTN)
|
XP_024308862.1:p.Glu33617=
|
|
XM_024453095.1:c.100848A>G
(TTN)
|
XP_024308863.1:p.Glu33616=
|
|
XM_024453096.1:c.100281A>G
(TTN)
|
XP_024308864.1:p.Glu33427=
|
|
XM_024453097.1:c.97623A>G
(TTN)
|
XP_024308865.1:p.Glu32541=
|
|
XM_024453098.1:c.97542A>G
(TTN)
|
XP_024308866.1:p.Glu32514=
|
|
XM_024453099.1:c.79305A>G
(TTN)
|
XP_024308867.1:p.Glu26435=
|
|
XM_024453100.1:c.69159A>G
(TTN)
|
XP_024308868.1:p.Glu23053=
|
|