ENST00000342992.11:c.52912A>G
(TTN)
|
ENSP00000343764.6:p.Asn17638Asp
|
|
ENST00000342175.11:c.33997A>G
(TTN)
|
ENSP00000340554.6:p.Asn11333Asp
|
|
ENST00000359218.10:c.33796A>G
(TTN)
|
ENSP00000352154.5:p.Asn11266Asp
|
|
ENST00000342175.10:c.33997A>G
(TTN)
|
ENSP00000340554.6:p.Asn11333Asp
|
|
ENST00000342992.10:c.52912A>G
(TTN)
|
ENSP00000343764.6:p.Asn17638Asp
|
|
ENST00000359218.9:c.33796A>G
(TTN)
|
ENSP00000352154.5:p.Asn11266Asp
|
|
ENST00000460472.6:c.33421A>G
(TTN)
|
ENSP00000434586.1:p.Asn11141Asp
|
|
ENST00000589042.5:c.60616A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn20206Asp
|
|
ENST00000591111.5:c.55693A>G
(TTN)
|
ENSP00000465570.1:p.Asn18565Asp
|
|
ENST00000615779.4:c.55693A>G
(TTN)
|
ENSP00000483597.1:p.Asn18565Asp
|
|
NM_001256850.1:c.55693A>G
(TTN)
|
NP_001243779.1:p.Asn18565Asp
|
|
NM_001267550.2:c.60616A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asn20206Asp
|
|
NM_003319.4:c.33421A>G
(TTN)
|
NP_003310.4:p.Asn11141Asp
|
|
NM_133378.4:c.52912A>G
(TTN)
|
NP_596869.4:p.Asn17638Asp
|
|
NM_133432.3:c.33796A>G
(TTN)
|
NP_597676.3:p.Asn11266Asp
|
|
NM_133437.4:c.33997A>G
(TTN)
|
NP_597681.4:p.Asn11333Asp
|
|
NR_038271.1:n.597-6487T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-30T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.59713A>G
(TTN)
|
XP_011510031.1:p.Asn19905Asp
|
|
XM_011511730.1:c.33607A>G
(TTN)
|
XP_011510032.1:p.Asn11203Asp
|
|
XM_011511731.1:c.33466A>G
(TTN)
|
XP_011510033.1:p.Asn11156Asp
|
|
XM_017004819.1:c.59509A>G
(TTN)
|
XP_016860308.1:p.Asn19837Asp
|
|
XM_017004820.1:c.54907A>G
(TTN)
|
XP_016860309.1:p.Asn18303Asp
|
|
XM_017004821.1:c.54904A>G
(TTN)
|
XP_016860310.1:p.Asn18302Asp
|
|
XM_017004822.1:c.51946A>G
(TTN)
|
XP_016860311.1:p.Asn17316Asp
|
|
XM_017004823.1:c.33562A>G
(TTN)
|
XP_016860312.1:p.Asn11188Asp
|
|
XM_024453094.1:c.55057A>G
(TTN)
|
XP_024308862.1:p.Asn18353Asp
|
|
XM_024453095.1:c.55054A>G
(TTN)
|
XP_024308863.1:p.Asn18352Asp
|
|
XM_024453096.1:c.54487A>G
(TTN)
|
XP_024308864.1:p.Asn18163Asp
|
|
XM_024453097.1:c.51829A>G
(TTN)
|
XP_024308865.1:p.Asn17277Asp
|
|
XM_024453098.1:c.51748A>G
(TTN)
|
XP_024308866.1:p.Asn17250Asp
|
|
XM_024453099.1:c.33511A>G
(TTN)
|
XP_024308867.1:p.Asn11171Asp
|
|
XM_024453100.1:c.23365A>G
(TTN)
|
XP_024308868.1:p.Asn7789Asp
|
|