ENST00000342992.11:c.83769C>A
(TTN)
|
ENSP00000343764.6:p.Arg27923=
|
|
ENST00000342175.11:c.64854C>A
(TTN)
|
ENSP00000340554.6:p.Arg21618=
|
|
ENST00000359218.10:c.64653C>A
(TTN)
|
ENSP00000352154.5:p.Arg21551=
|
|
ENST00000342175.10:c.64854C>A
(TTN)
|
ENSP00000340554.6:p.Arg21618=
|
|
ENST00000342992.10:c.83769C>A
(TTN)
|
ENSP00000343764.6:p.Arg27923=
|
|
ENST00000359218.9:c.64653C>A
(TTN)
|
ENSP00000352154.5:p.Arg21551=
|
|
ENST00000460472.6:c.64278C>A
(TTN)
|
ENSP00000434586.1:p.Arg21426=
|
|
ENST00000589042.5:c.91473C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg30491=
|
|
ENST00000591111.5:c.86550C>A
(TTN)
|
ENSP00000465570.1:p.Arg28850=
|
|
ENST00000615779.4:c.86550C>A
(TTN)
|
ENSP00000483597.1:p.Arg28850=
|
|
NM_001256850.1:c.86550C>A
(TTN)
|
NP_001243779.1:p.Arg28850=
|
|
NM_001267550.2:c.91473C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Arg30491=
|
|
NM_003319.4:c.64278C>A
(TTN)
|
NP_003310.4:p.Arg21426=
|
|
NM_133378.4:c.83769C>A
(TTN)
|
NP_596869.4:p.Arg27923=
|
|
NM_133432.3:c.64653C>A
(TTN)
|
NP_597676.3:p.Arg21551=
|
|
NM_133437.4:c.64854C>A
(TTN)
|
NP_597681.4:p.Arg21618=
|
|
NR_038271.1:n.447-20242G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+8697G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.90570C>A
(TTN)
|
XP_011510031.1:p.Arg30190=
|
|
XM_011511730.1:c.64464C>A
(TTN)
|
XP_011510032.1:p.Arg21488=
|
|
XM_011511731.1:c.64323C>A
(TTN)
|
XP_011510033.1:p.Arg21441=
|
|
XM_017004819.1:c.90366C>A
(TTN)
|
XP_016860308.1:p.Arg30122=
|
|
XM_017004820.1:c.85764C>A
(TTN)
|
XP_016860309.1:p.Arg28588=
|
|
XM_017004821.1:c.85761C>A
(TTN)
|
XP_016860310.1:p.Arg28587=
|
|
XM_017004822.1:c.82803C>A
(TTN)
|
XP_016860311.1:p.Arg27601=
|
|
XM_017004823.1:c.64419C>A
(TTN)
|
XP_016860312.1:p.Arg21473=
|
|
XM_024453094.1:c.85914C>A
(TTN)
|
XP_024308862.1:p.Arg28638=
|
|
XM_024453095.1:c.85911C>A
(TTN)
|
XP_024308863.1:p.Arg28637=
|
|
XM_024453096.1:c.85344C>A
(TTN)
|
XP_024308864.1:p.Arg28448=
|
|
XM_024453097.1:c.82686C>A
(TTN)
|
XP_024308865.1:p.Arg27562=
|
|
XM_024453098.1:c.82605C>A
(TTN)
|
XP_024308866.1:p.Arg27535=
|
|
XM_024453099.1:c.64368C>A
(TTN)
|
XP_024308867.1:p.Arg21456=
|
|
XM_024453100.1:c.54222C>A
(TTN)
|
XP_024308868.1:p.Arg18074=
|
|