ENST00000342992.11:c.83514C>A
(TTN)
|
ENSP00000343764.6:p.Gly27838=
|
|
ENST00000342175.11:c.64599C>A
(TTN)
|
ENSP00000340554.6:p.Gly21533=
|
|
ENST00000359218.10:c.64398C>A
(TTN)
|
ENSP00000352154.5:p.Gly21466=
|
|
ENST00000342175.10:c.64599C>A
(TTN)
|
ENSP00000340554.6:p.Gly21533=
|
|
ENST00000342992.10:c.83514C>A
(TTN)
|
ENSP00000343764.6:p.Gly27838=
|
|
ENST00000359218.9:c.64398C>A
(TTN)
|
ENSP00000352154.5:p.Gly21466=
|
|
ENST00000460472.6:c.64023C>A
(TTN)
|
ENSP00000434586.1:p.Gly21341=
|
|
ENST00000589042.5:c.91218C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly30406=
|
|
ENST00000591111.5:c.86295C>A
(TTN)
|
ENSP00000465570.1:p.Gly28765=
|
|
ENST00000615779.4:c.86295C>A
(TTN)
|
ENSP00000483597.1:p.Gly28765=
|
|
NM_001256850.1:c.86295C>A
(TTN)
|
NP_001243779.1:p.Gly28765=
|
|
NM_001267550.2:c.91218C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly30406=
|
|
NM_003319.4:c.64023C>A
(TTN)
|
NP_003310.4:p.Gly21341=
|
|
NM_133378.4:c.83514C>A
(TTN)
|
NP_596869.4:p.Gly27838=
|
|
NM_133432.3:c.64398C>A
(TTN)
|
NP_597676.3:p.Gly21466=
|
|
NM_133437.4:c.64599C>A
(TTN)
|
NP_597681.4:p.Gly21533=
|
|
NR_038271.1:n.447-19618G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9321G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.90315C>A
(TTN)
|
XP_011510031.1:p.Gly30105=
|
|
XM_011511730.1:c.64209C>A
(TTN)
|
XP_011510032.1:p.Gly21403=
|
|
XM_011511731.1:c.64068C>A
(TTN)
|
XP_011510033.1:p.Gly21356=
|
|
XM_017004819.1:c.90111C>A
(TTN)
|
XP_016860308.1:p.Gly30037=
|
|
XM_017004820.1:c.85509C>A
(TTN)
|
XP_016860309.1:p.Gly28503=
|
|
XM_017004821.1:c.85506C>A
(TTN)
|
XP_016860310.1:p.Gly28502=
|
|
XM_017004822.1:c.82548C>A
(TTN)
|
XP_016860311.1:p.Gly27516=
|
|
XM_017004823.1:c.64164C>A
(TTN)
|
XP_016860312.1:p.Gly21388=
|
|
XM_024453094.1:c.85659C>A
(TTN)
|
XP_024308862.1:p.Gly28553=
|
|
XM_024453095.1:c.85656C>A
(TTN)
|
XP_024308863.1:p.Gly28552=
|
|
XM_024453096.1:c.85089C>A
(TTN)
|
XP_024308864.1:p.Gly28363=
|
|
XM_024453097.1:c.82431C>A
(TTN)
|
XP_024308865.1:p.Gly27477=
|
|
XM_024453098.1:c.82350C>A
(TTN)
|
XP_024308866.1:p.Gly27450=
|
|
XM_024453099.1:c.64113C>A
(TTN)
|
XP_024308867.1:p.Gly21371=
|
|
XM_024453100.1:c.53967C>A
(TTN)
|
XP_024308868.1:p.Gly17989=
|
|