ENST00000342992.11:c.98318C>A
(TTN)
|
ENSP00000343764.6:p.Thr32773Asn
|
|
ENST00000342175.11:c.79403C>A
(TTN)
|
ENSP00000340554.6:p.Thr26468Asn
|
|
ENST00000359218.10:c.79202C>A
(TTN)
|
ENSP00000352154.5:p.Thr26401Asn
|
|
ENST00000342175.10:c.79403C>A
(TTN)
|
ENSP00000340554.6:p.Thr26468Asn
|
|
ENST00000342992.10:c.98318C>A
(TTN)
|
ENSP00000343764.6:p.Thr32773Asn
|
|
ENST00000359218.9:c.79202C>A
(TTN)
|
ENSP00000352154.5:p.Thr26401Asn
|
|
ENST00000460472.6:c.78827C>A
(TTN)
|
ENSP00000434586.1:p.Thr26276Asn
|
|
ENST00000589042.5:c.106022C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35341Asn
|
|
ENST00000591111.5:c.101099C>A
(TTN)
|
ENSP00000465570.1:p.Thr33700Asn
|
|
ENST00000615779.4:c.101099C>A
(TTN)
|
ENSP00000483597.1:p.Thr33700Asn
|
|
NM_001256850.1:c.101099C>A
(TTN)
|
NP_001243779.1:p.Thr33700Asn
|
|
NM_001267550.2:c.106022C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35341Asn
|
|
NM_003319.4:c.78827C>A
(TTN)
|
NP_003310.4:p.Thr26276Asn
|
|
NM_133378.4:c.98318C>A
(TTN)
|
NP_596869.4:p.Thr32773Asn
|
|
NM_133432.3:c.79202C>A
(TTN)
|
NP_597676.3:p.Thr26401Asn
|
|
NM_133437.4:c.79403C>A
(TTN)
|
NP_597681.4:p.Thr26468Asn
|
|
NR_038271.1:n.446+6957G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5139G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105119C>A
(TTN)
|
XP_011510031.1:p.Thr35040Asn
|
|
XM_011511730.1:c.79013C>A
(TTN)
|
XP_011510032.1:p.Thr26338Asn
|
|
XM_011511731.1:c.78872C>A
(TTN)
|
XP_011510033.1:p.Thr26291Asn
|
|
XM_017004819.1:c.104915C>A
(TTN)
|
XP_016860308.1:p.Thr34972Asn
|
|
XM_017004820.1:c.100313C>A
(TTN)
|
XP_016860309.1:p.Thr33438Asn
|
|
XM_017004821.1:c.100310C>A
(TTN)
|
XP_016860310.1:p.Thr33437Asn
|
|
XM_017004822.1:c.97352C>A
(TTN)
|
XP_016860311.1:p.Thr32451Asn
|
|
XM_017004823.1:c.78968C>A
(TTN)
|
XP_016860312.1:p.Thr26323Asn
|
|
XM_024453094.1:c.100463C>A
(TTN)
|
XP_024308862.1:p.Thr33488Asn
|
|
XM_024453095.1:c.100460C>A
(TTN)
|
XP_024308863.1:p.Thr33487Asn
|
|
XM_024453096.1:c.99893C>A
(TTN)
|
XP_024308864.1:p.Thr33298Asn
|
|
XM_024453097.1:c.97235C>A
(TTN)
|
XP_024308865.1:p.Thr32412Asn
|
|
XM_024453098.1:c.97154C>A
(TTN)
|
XP_024308866.1:p.Thr32385Asn
|
|
XM_024453099.1:c.78917C>A
(TTN)
|
XP_024308867.1:p.Thr26306Asn
|
|
XM_024453100.1:c.68771C>A
(TTN)
|
XP_024308868.1:p.Thr22924Asn
|
|