ENST00000342992.11:c.51635G>A
(TTN)
|
ENSP00000343764.6:p.Arg17212Lys
|
|
ENST00000342175.11:c.32720G>A
(TTN)
|
ENSP00000340554.6:p.Arg10907Lys
|
|
ENST00000359218.10:c.32519G>A
(TTN)
|
ENSP00000352154.5:p.Arg10840Lys
|
|
ENST00000342175.10:c.32720G>A
(TTN)
|
ENSP00000340554.6:p.Arg10907Lys
|
|
ENST00000342992.10:c.51635G>A
(TTN)
|
ENSP00000343764.6:p.Arg17212Lys
|
|
ENST00000359218.9:c.32519G>A
(TTN)
|
ENSP00000352154.5:p.Arg10840Lys
|
|
ENST00000460472.6:c.32144G>A
(TTN)
|
ENSP00000434586.1:p.Arg10715Lys
|
|
ENST00000589042.5:c.59339G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg19780Lys
|
|
ENST00000591111.5:c.54416G>A
(TTN)
|
ENSP00000465570.1:p.Arg18139Lys
|
|
ENST00000615779.4:c.54416G>A
(TTN)
|
ENSP00000483597.1:p.Arg18139Lys
|
|
NM_001256850.1:c.54416G>A
(TTN)
|
NP_001243779.1:p.Arg18139Lys
|
|
NM_001267550.2:c.59339G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Arg19780Lys
|
|
NM_003319.4:c.32144G>A
(TTN)
|
NP_003310.4:p.Arg10715Lys
|
|
NM_133378.4:c.51635G>A
(TTN)
|
NP_596869.4:p.Arg17212Lys
|
|
NM_133432.3:c.32519G>A
(TTN)
|
NP_597676.3:p.Arg10840Lys
|
|
NM_133437.4:c.32720G>A
(TTN)
|
NP_597681.4:p.Arg10907Lys
|
|
NR_038271.1:n.597-4816C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1466C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.58436G>A
(TTN)
|
XP_011510031.1:p.Arg19479Lys
|
|
XM_011511730.1:c.32330G>A
(TTN)
|
XP_011510032.1:p.Arg10777Lys
|
|
XM_011511731.1:c.32189G>A
(TTN)
|
XP_011510033.1:p.Arg10730Lys
|
|
XM_017004819.1:c.58232G>A
(TTN)
|
XP_016860308.1:p.Arg19411Lys
|
|
XM_017004820.1:c.53630G>A
(TTN)
|
XP_016860309.1:p.Arg17877Lys
|
|
XM_017004821.1:c.53627G>A
(TTN)
|
XP_016860310.1:p.Arg17876Lys
|
|
XM_017004822.1:c.50669G>A
(TTN)
|
XP_016860311.1:p.Arg16890Lys
|
|
XM_017004823.1:c.32285G>A
(TTN)
|
XP_016860312.1:p.Arg10762Lys
|
|
XM_024453094.1:c.53780G>A
(TTN)
|
XP_024308862.1:p.Arg17927Lys
|
|
XM_024453095.1:c.53777G>A
(TTN)
|
XP_024308863.1:p.Arg17926Lys
|
|
XM_024453096.1:c.53210G>A
(TTN)
|
XP_024308864.1:p.Arg17737Lys
|
|
XM_024453097.1:c.50552G>A
(TTN)
|
XP_024308865.1:p.Arg16851Lys
|
|
XM_024453098.1:c.50471G>A
(TTN)
|
XP_024308866.1:p.Arg16824Lys
|
|
XM_024453099.1:c.32234G>A
(TTN)
|
XP_024308867.1:p.Arg10745Lys
|
|
XM_024453100.1:c.22088G>A
(TTN)
|
XP_024308868.1:p.Arg7363Lys
|
|