ENST00000342992.11:c.98282A>C
(TTN)
|
ENSP00000343764.6:p.Asn32761Thr
|
|
ENST00000342175.11:c.79367A>C
(TTN)
|
ENSP00000340554.6:p.Asn26456Thr
|
|
ENST00000359218.10:c.79166A>C
(TTN)
|
ENSP00000352154.5:p.Asn26389Thr
|
|
ENST00000342175.10:c.79367A>C
(TTN)
|
ENSP00000340554.6:p.Asn26456Thr
|
|
ENST00000342992.10:c.98282A>C
(TTN)
|
ENSP00000343764.6:p.Asn32761Thr
|
|
ENST00000359218.9:c.79166A>C
(TTN)
|
ENSP00000352154.5:p.Asn26389Thr
|
|
ENST00000460472.6:c.78791A>C
(TTN)
|
ENSP00000434586.1:p.Asn26264Thr
|
|
ENST00000589042.5:c.105986A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn35329Thr
|
|
ENST00000591111.5:c.101063A>C
(TTN)
|
ENSP00000465570.1:p.Asn33688Thr
|
|
ENST00000615779.4:c.101063A>C
(TTN)
|
ENSP00000483597.1:p.Asn33688Thr
|
|
NM_001256850.1:c.101063A>C
(TTN)
|
NP_001243779.1:p.Asn33688Thr
|
|
NM_001267550.2:c.105986A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asn35329Thr
|
|
NM_003319.4:c.78791A>C
(TTN)
|
NP_003310.4:p.Asn26264Thr
|
|
NM_133378.4:c.98282A>C
(TTN)
|
NP_596869.4:p.Asn32761Thr
|
|
NM_133432.3:c.79166A>C
(TTN)
|
NP_597676.3:p.Asn26389Thr
|
|
NM_133437.4:c.79367A>C
(TTN)
|
NP_597681.4:p.Asn26456Thr
|
|
NR_038271.1:n.446+6993T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5103T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105083A>C
(TTN)
|
XP_011510031.1:p.Asn35028Thr
|
|
XM_011511730.1:c.78977A>C
(TTN)
|
XP_011510032.1:p.Asn26326Thr
|
|
XM_011511731.1:c.78836A>C
(TTN)
|
XP_011510033.1:p.Asn26279Thr
|
|
XM_017004819.1:c.104879A>C
(TTN)
|
XP_016860308.1:p.Asn34960Thr
|
|
XM_017004820.1:c.100277A>C
(TTN)
|
XP_016860309.1:p.Asn33426Thr
|
|
XM_017004821.1:c.100274A>C
(TTN)
|
XP_016860310.1:p.Asn33425Thr
|
|
XM_017004822.1:c.97316A>C
(TTN)
|
XP_016860311.1:p.Asn32439Thr
|
|
XM_017004823.1:c.78932A>C
(TTN)
|
XP_016860312.1:p.Asn26311Thr
|
|
XM_024453094.1:c.100427A>C
(TTN)
|
XP_024308862.1:p.Asn33476Thr
|
|
XM_024453095.1:c.100424A>C
(TTN)
|
XP_024308863.1:p.Asn33475Thr
|
|
XM_024453096.1:c.99857A>C
(TTN)
|
XP_024308864.1:p.Asn33286Thr
|
|
XM_024453097.1:c.97199A>C
(TTN)
|
XP_024308865.1:p.Asn32400Thr
|
|
XM_024453098.1:c.97118A>C
(TTN)
|
XP_024308866.1:p.Asn32373Thr
|
|
XM_024453099.1:c.78881A>C
(TTN)
|
XP_024308867.1:p.Asn26294Thr
|
|
XM_024453100.1:c.68735A>C
(TTN)
|
XP_024308868.1:p.Asn22912Thr
|
|