ENST00000342992.11:c.52912A>T
(TTN)
|
ENSP00000343764.6:p.Asn17638Tyr
|
|
ENST00000342175.11:c.33997A>T
(TTN)
|
ENSP00000340554.6:p.Asn11333Tyr
|
|
ENST00000359218.10:c.33796A>T
(TTN)
|
ENSP00000352154.5:p.Asn11266Tyr
|
|
ENST00000342175.10:c.33997A>T
(TTN)
|
ENSP00000340554.6:p.Asn11333Tyr
|
|
ENST00000342992.10:c.52912A>T
(TTN)
|
ENSP00000343764.6:p.Asn17638Tyr
|
|
ENST00000359218.9:c.33796A>T
(TTN)
|
ENSP00000352154.5:p.Asn11266Tyr
|
|
ENST00000460472.6:c.33421A>T
(TTN)
|
ENSP00000434586.1:p.Asn11141Tyr
|
|
ENST00000589042.5:c.60616A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn20206Tyr
|
|
ENST00000591111.5:c.55693A>T
(TTN)
|
ENSP00000465570.1:p.Asn18565Tyr
|
|
ENST00000615779.4:c.55693A>T
(TTN)
|
ENSP00000483597.1:p.Asn18565Tyr
|
|
NM_001256850.1:c.55693A>T
(TTN)
|
NP_001243779.1:p.Asn18565Tyr
|
|
NM_001267550.2:c.60616A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asn20206Tyr
|
|
NM_003319.4:c.33421A>T
(TTN)
|
NP_003310.4:p.Asn11141Tyr
|
|
NM_133378.4:c.52912A>T
(TTN)
|
NP_596869.4:p.Asn17638Tyr
|
|
NM_133432.3:c.33796A>T
(TTN)
|
NP_597676.3:p.Asn11266Tyr
|
|
NM_133437.4:c.33997A>T
(TTN)
|
NP_597681.4:p.Asn11333Tyr
|
|
NR_038271.1:n.597-6487T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-30T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.59713A>T
(TTN)
|
XP_011510031.1:p.Asn19905Tyr
|
|
XM_011511730.1:c.33607A>T
(TTN)
|
XP_011510032.1:p.Asn11203Tyr
|
|
XM_011511731.1:c.33466A>T
(TTN)
|
XP_011510033.1:p.Asn11156Tyr
|
|
XM_017004819.1:c.59509A>T
(TTN)
|
XP_016860308.1:p.Asn19837Tyr
|
|
XM_017004820.1:c.54907A>T
(TTN)
|
XP_016860309.1:p.Asn18303Tyr
|
|
XM_017004821.1:c.54904A>T
(TTN)
|
XP_016860310.1:p.Asn18302Tyr
|
|
XM_017004822.1:c.51946A>T
(TTN)
|
XP_016860311.1:p.Asn17316Tyr
|
|
XM_017004823.1:c.33562A>T
(TTN)
|
XP_016860312.1:p.Asn11188Tyr
|
|
XM_024453094.1:c.55057A>T
(TTN)
|
XP_024308862.1:p.Asn18353Tyr
|
|
XM_024453095.1:c.55054A>T
(TTN)
|
XP_024308863.1:p.Asn18352Tyr
|
|
XM_024453096.1:c.54487A>T
(TTN)
|
XP_024308864.1:p.Asn18163Tyr
|
|
XM_024453097.1:c.51829A>T
(TTN)
|
XP_024308865.1:p.Asn17277Tyr
|
|
XM_024453098.1:c.51748A>T
(TTN)
|
XP_024308866.1:p.Asn17250Tyr
|
|
XM_024453099.1:c.33511A>T
(TTN)
|
XP_024308867.1:p.Asn11171Tyr
|
|
XM_024453100.1:c.23365A>T
(TTN)
|
XP_024308868.1:p.Asn7789Tyr
|
|