ENST00000342992.11:c.56749C>A
(TTN)
|
ENSP00000343764.6:p.Arg18917=
|
|
ENST00000342175.11:c.37834C>A
(TTN)
|
ENSP00000340554.6:p.Arg12612=
|
|
ENST00000359218.10:c.37633C>A
(TTN)
|
ENSP00000352154.5:p.Arg12545=
|
|
ENST00000342175.10:c.37834C>A
(TTN)
|
ENSP00000340554.6:p.Arg12612=
|
|
ENST00000342992.10:c.56749C>A
(TTN)
|
ENSP00000343764.6:p.Arg18917=
|
|
ENST00000359218.9:c.37633C>A
(TTN)
|
ENSP00000352154.5:p.Arg12545=
|
|
ENST00000460472.6:c.37258C>A
(TTN)
|
ENSP00000434586.1:p.Arg12420=
|
|
ENST00000589042.5:c.64453C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg21485=
|
|
ENST00000591111.5:c.59530C>A
(TTN)
|
ENSP00000465570.1:p.Arg19844=
|
|
ENST00000615779.4:c.59530C>A
(TTN)
|
ENSP00000483597.1:p.Arg19844=
|
|
NM_001256850.1:c.59530C>A
(TTN)
|
NP_001243779.1:p.Arg19844=
|
|
NM_001267550.2:c.64453C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Arg21485=
|
|
NM_003319.4:c.37258C>A
(TTN)
|
NP_003310.4:p.Arg12420=
|
|
NM_133378.4:c.56749C>A
(TTN)
|
NP_596869.4:p.Arg18917=
|
|
NM_133432.3:c.37633C>A
(TTN)
|
NP_597676.3:p.Arg12545=
|
|
NM_133437.4:c.37834C>A
(TTN)
|
NP_597681.4:p.Arg12612=
|
|
NR_038271.1:n.597-12305G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3188+298G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.63550C>A
(TTN)
|
XP_011510031.1:p.Arg21184=
|
|
XM_011511730.1:c.37444C>A
(TTN)
|
XP_011510032.1:p.Arg12482=
|
|
XM_011511731.1:c.37303C>A
(TTN)
|
XP_011510033.1:p.Arg12435=
|
|
XM_017004819.1:c.63346C>A
(TTN)
|
XP_016860308.1:p.Arg21116=
|
|
XM_017004820.1:c.58744C>A
(TTN)
|
XP_016860309.1:p.Arg19582=
|
|
XM_017004821.1:c.58741C>A
(TTN)
|
XP_016860310.1:p.Arg19581=
|
|
XM_017004822.1:c.55783C>A
(TTN)
|
XP_016860311.1:p.Arg18595=
|
|
XM_017004823.1:c.37399C>A
(TTN)
|
XP_016860312.1:p.Arg12467=
|
|
XM_024453094.1:c.58894C>A
(TTN)
|
XP_024308862.1:p.Arg19632=
|
|
XM_024453095.1:c.58891C>A
(TTN)
|
XP_024308863.1:p.Arg19631=
|
|
XM_024453096.1:c.58324C>A
(TTN)
|
XP_024308864.1:p.Arg19442=
|
|
XM_024453097.1:c.55666C>A
(TTN)
|
XP_024308865.1:p.Arg18556=
|
|
XM_024453098.1:c.55585C>A
(TTN)
|
XP_024308866.1:p.Arg18529=
|
|
XM_024453099.1:c.37348C>A
(TTN)
|
XP_024308867.1:p.Arg12450=
|
|
XM_024453100.1:c.27202C>A
(TTN)
|
XP_024308868.1:p.Arg9068=
|
|