ENST00000342992.11:c.49968T>G
(TTN)
|
ENSP00000343764.6:p.Arg16656=
|
|
ENST00000342175.11:c.31053T>G
(TTN)
|
ENSP00000340554.6:p.Arg10351=
|
|
ENST00000359218.10:c.30852T>G
(TTN)
|
ENSP00000352154.5:p.Arg10284=
|
|
ENST00000342175.10:c.31053T>G
(TTN)
|
ENSP00000340554.6:p.Arg10351=
|
|
ENST00000342992.10:c.49968T>G
(TTN)
|
ENSP00000343764.6:p.Arg16656=
|
|
ENST00000359218.9:c.30852T>G
(TTN)
|
ENSP00000352154.5:p.Arg10284=
|
|
ENST00000460472.6:c.30477T>G
(TTN)
|
ENSP00000434586.1:p.Arg10159=
|
|
ENST00000589042.5:c.57672T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg19224=
|
|
ENST00000591111.5:c.52749T>G
(TTN)
|
ENSP00000465570.1:p.Arg17583=
|
|
ENST00000615779.4:c.52749T>G
(TTN)
|
ENSP00000483597.1:p.Arg17583=
|
|
NM_001256850.1:c.52749T>G
(TTN)
|
NP_001243779.1:p.Arg17583=
|
|
NM_001267550.2:c.57672T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Arg19224=
|
|
NM_003319.4:c.30477T>G
(TTN)
|
NP_003310.4:p.Arg10159=
|
|
NM_133378.4:c.49968T>G
(TTN)
|
NP_596869.4:p.Arg16656=
|
|
NM_133432.3:c.30852T>G
(TTN)
|
NP_597676.3:p.Arg10284=
|
|
NM_133437.4:c.31053T>G
(TTN)
|
NP_597681.4:p.Arg10351=
|
|
NR_038271.1:n.597-1914A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3365-1914A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.56769T>G
(TTN)
|
XP_011510031.1:p.Arg18923=
|
|
XM_011511730.1:c.30663T>G
(TTN)
|
XP_011510032.1:p.Arg10221=
|
|
XM_011511731.1:c.30522T>G
(TTN)
|
XP_011510033.1:p.Arg10174=
|
|
XM_017004819.1:c.56565T>G
(TTN)
|
XP_016860308.1:p.Arg18855=
|
|
XM_017004820.1:c.51963T>G
(TTN)
|
XP_016860309.1:p.Arg17321=
|
|
XM_017004821.1:c.51960T>G
(TTN)
|
XP_016860310.1:p.Arg17320=
|
|
XM_017004822.1:c.49002T>G
(TTN)
|
XP_016860311.1:p.Arg16334=
|
|
XM_017004823.1:c.30618T>G
(TTN)
|
XP_016860312.1:p.Arg10206=
|
|
XM_024453094.1:c.52113T>G
(TTN)
|
XP_024308862.1:p.Arg17371=
|
|
XM_024453095.1:c.52110T>G
(TTN)
|
XP_024308863.1:p.Arg17370=
|
|
XM_024453096.1:c.51543T>G
(TTN)
|
XP_024308864.1:p.Arg17181=
|
|
XM_024453097.1:c.48885T>G
(TTN)
|
XP_024308865.1:p.Arg16295=
|
|
XM_024453098.1:c.48804T>G
(TTN)
|
XP_024308866.1:p.Arg16268=
|
|
XM_024453099.1:c.30567T>G
(TTN)
|
XP_024308867.1:p.Arg10189=
|
|
XM_024453100.1:c.20421T>G
(TTN)
|
XP_024308868.1:p.Arg6807=
|
|