ENST00000342992.11:c.64561A>G
(TTN)
|
ENSP00000343764.6:p.Asn21521Asp
|
|
ENST00000342175.11:c.45646A>G
(TTN)
|
ENSP00000340554.6:p.Asn15216Asp
|
|
ENST00000359218.10:c.45445A>G
(TTN)
|
ENSP00000352154.5:p.Asn15149Asp
|
|
ENST00000342175.10:c.45646A>G
(TTN)
|
ENSP00000340554.6:p.Asn15216Asp
|
|
ENST00000342992.10:c.64561A>G
(TTN)
|
ENSP00000343764.6:p.Asn21521Asp
|
|
ENST00000359218.9:c.45445A>G
(TTN)
|
ENSP00000352154.5:p.Asn15149Asp
|
|
ENST00000460472.6:c.45070A>G
(TTN)
|
ENSP00000434586.1:p.Asn15024Asp
|
|
ENST00000589042.5:c.72265A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn24089Asp
|
|
ENST00000591111.5:c.67342A>G
(TTN)
|
ENSP00000465570.1:p.Asn22448Asp
|
|
ENST00000615779.4:c.67342A>G
(TTN)
|
ENSP00000483597.1:p.Asn22448Asp
|
|
NM_001256850.1:c.67342A>G
(TTN)
|
NP_001243779.1:p.Asn22448Asp
|
|
NM_001267550.2:c.72265A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asn24089Asp
|
|
NM_003319.4:c.45070A>G
(TTN)
|
NP_003310.4:p.Asn15024Asp
|
|
NM_133378.4:c.64561A>G
(TTN)
|
NP_596869.4:p.Asn21521Asp
|
|
NM_133432.3:c.45445A>G
(TTN)
|
NP_597676.3:p.Asn15149Asp
|
|
NM_133437.4:c.45646A>G
(TTN)
|
NP_597681.4:p.Asn15216Asp
|
|
NR_038271.1:n.596+2418T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-8705T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.71362A>G
(TTN)
|
XP_011510031.1:p.Asn23788Asp
|
|
XM_011511730.1:c.45256A>G
(TTN)
|
XP_011510032.1:p.Asn15086Asp
|
|
XM_011511731.1:c.45115A>G
(TTN)
|
XP_011510033.1:p.Asn15039Asp
|
|
XM_017004819.1:c.71158A>G
(TTN)
|
XP_016860308.1:p.Asn23720Asp
|
|
XM_017004820.1:c.66556A>G
(TTN)
|
XP_016860309.1:p.Asn22186Asp
|
|
XM_017004821.1:c.66553A>G
(TTN)
|
XP_016860310.1:p.Asn22185Asp
|
|
XM_017004822.1:c.63595A>G
(TTN)
|
XP_016860311.1:p.Asn21199Asp
|
|
XM_017004823.1:c.45211A>G
(TTN)
|
XP_016860312.1:p.Asn15071Asp
|
|
XM_024453094.1:c.66706A>G
(TTN)
|
XP_024308862.1:p.Asn22236Asp
|
|
XM_024453095.1:c.66703A>G
(TTN)
|
XP_024308863.1:p.Asn22235Asp
|
|
XM_024453096.1:c.66136A>G
(TTN)
|
XP_024308864.1:p.Asn22046Asp
|
|
XM_024453097.1:c.63478A>G
(TTN)
|
XP_024308865.1:p.Asn21160Asp
|
|
XM_024453098.1:c.63397A>G
(TTN)
|
XP_024308866.1:p.Asn21133Asp
|
|
XM_024453099.1:c.45160A>G
(TTN)
|
XP_024308867.1:p.Asn15054Asp
|
|
XM_024453100.1:c.35014A>G
(TTN)
|
XP_024308868.1:p.Asn11672Asp
|
|