ENST00000342992.11:c.67873A>G
(TTN)
|
ENSP00000343764.6:p.Arg22625Gly
|
|
ENST00000342175.11:c.48958A>G
(TTN)
|
ENSP00000340554.6:p.Arg16320Gly
|
|
ENST00000359218.10:c.48757A>G
(TTN)
|
ENSP00000352154.5:p.Arg16253Gly
|
|
ENST00000342175.10:c.48958A>G
(TTN)
|
ENSP00000340554.6:p.Arg16320Gly
|
|
ENST00000342992.10:c.67873A>G
(TTN)
|
ENSP00000343764.6:p.Arg22625Gly
|
|
ENST00000359218.9:c.48757A>G
(TTN)
|
ENSP00000352154.5:p.Arg16253Gly
|
|
ENST00000460472.6:c.48382A>G
(TTN)
|
ENSP00000434586.1:p.Arg16128Gly
|
|
ENST00000589042.5:c.75577A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg25193Gly
|
|
ENST00000591111.5:c.70654A>G
(TTN)
|
ENSP00000465570.1:p.Arg23552Gly
|
|
ENST00000615779.4:c.70654A>G
(TTN)
|
ENSP00000483597.1:p.Arg23552Gly
|
|
NM_001256850.1:c.70654A>G
(TTN)
|
NP_001243779.1:p.Arg23552Gly
|
|
NM_001267550.2:c.75577A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Arg25193Gly
|
|
NM_003319.4:c.48382A>G
(TTN)
|
NP_003310.4:p.Arg16128Gly
|
|
NM_133378.4:c.67873A>G
(TTN)
|
NP_596869.4:p.Arg22625Gly
|
|
NM_133432.3:c.48757A>G
(TTN)
|
NP_597676.3:p.Arg16253Gly
|
|
NM_133437.4:c.48958A>G
(TTN)
|
NP_597681.4:p.Arg16320Gly
|
|
NR_038271.1:n.447-745T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12017T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.74674A>G
(TTN)
|
XP_011510031.1:p.Arg24892Gly
|
|
XM_011511730.1:c.48568A>G
(TTN)
|
XP_011510032.1:p.Arg16190Gly
|
|
XM_011511731.1:c.48427A>G
(TTN)
|
XP_011510033.1:p.Arg16143Gly
|
|
XM_017004819.1:c.74470A>G
(TTN)
|
XP_016860308.1:p.Arg24824Gly
|
|
XM_017004820.1:c.69868A>G
(TTN)
|
XP_016860309.1:p.Arg23290Gly
|
|
XM_017004821.1:c.69865A>G
(TTN)
|
XP_016860310.1:p.Arg23289Gly
|
|
XM_017004822.1:c.66907A>G
(TTN)
|
XP_016860311.1:p.Arg22303Gly
|
|
XM_017004823.1:c.48523A>G
(TTN)
|
XP_016860312.1:p.Arg16175Gly
|
|
XM_024453094.1:c.70018A>G
(TTN)
|
XP_024308862.1:p.Arg23340Gly
|
|
XM_024453095.1:c.70015A>G
(TTN)
|
XP_024308863.1:p.Arg23339Gly
|
|
XM_024453096.1:c.69448A>G
(TTN)
|
XP_024308864.1:p.Arg23150Gly
|
|
XM_024453097.1:c.66790A>G
(TTN)
|
XP_024308865.1:p.Arg22264Gly
|
|
XM_024453098.1:c.66709A>G
(TTN)
|
XP_024308866.1:p.Arg22237Gly
|
|
XM_024453099.1:c.48472A>G
(TTN)
|
XP_024308867.1:p.Arg16158Gly
|
|
XM_024453100.1:c.38326A>G
(TTN)
|
XP_024308868.1:p.Arg12776Gly
|
|