ENST00000342992.11:c.57368T>A
(TTN)
|
ENSP00000343764.6:p.Ile19123Asn
|
|
ENST00000342175.11:c.38453T>A
(TTN)
|
ENSP00000340554.6:p.Ile12818Asn
|
|
ENST00000359218.10:c.38252T>A
(TTN)
|
ENSP00000352154.5:p.Ile12751Asn
|
|
ENST00000342175.10:c.38453T>A
(TTN)
|
ENSP00000340554.6:p.Ile12818Asn
|
|
ENST00000342992.10:c.57368T>A
(TTN)
|
ENSP00000343764.6:p.Ile19123Asn
|
|
ENST00000359218.9:c.38252T>A
(TTN)
|
ENSP00000352154.5:p.Ile12751Asn
|
|
ENST00000460472.6:c.37877T>A
(TTN)
|
ENSP00000434586.1:p.Ile12626Asn
|
|
ENST00000589042.5:c.65072T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile21691Asn
|
|
ENST00000591111.5:c.60149T>A
(TTN)
|
ENSP00000465570.1:p.Ile20050Asn
|
|
ENST00000615779.4:c.60149T>A
(TTN)
|
ENSP00000483597.1:p.Ile20050Asn
|
|
NM_001256850.1:c.60149T>A
(TTN)
|
NP_001243779.1:p.Ile20050Asn
|
|
NM_001267550.2:c.65072T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ile21691Asn
|
|
NM_003319.4:c.37877T>A
(TTN)
|
NP_003310.4:p.Ile12626Asn
|
|
NM_133378.4:c.57368T>A
(TTN)
|
NP_596869.4:p.Ile19123Asn
|
|
NM_133432.3:c.38252T>A
(TTN)
|
NP_597676.3:p.Ile12751Asn
|
|
NM_133437.4:c.38453T>A
(TTN)
|
NP_597681.4:p.Ile12818Asn
|
|
NR_038271.1:n.596+13030A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2768-94A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.64169T>A
(TTN)
|
XP_011510031.1:p.Ile21390Asn
|
|
XM_011511730.1:c.38063T>A
(TTN)
|
XP_011510032.1:p.Ile12688Asn
|
|
XM_011511731.1:c.37922T>A
(TTN)
|
XP_011510033.1:p.Ile12641Asn
|
|
XM_017004819.1:c.63965T>A
(TTN)
|
XP_016860308.1:p.Ile21322Asn
|
|
XM_017004820.1:c.59363T>A
(TTN)
|
XP_016860309.1:p.Ile19788Asn
|
|
XM_017004821.1:c.59360T>A
(TTN)
|
XP_016860310.1:p.Ile19787Asn
|
|
XM_017004822.1:c.56402T>A
(TTN)
|
XP_016860311.1:p.Ile18801Asn
|
|
XM_017004823.1:c.38018T>A
(TTN)
|
XP_016860312.1:p.Ile12673Asn
|
|
XM_024453094.1:c.59513T>A
(TTN)
|
XP_024308862.1:p.Ile19838Asn
|
|
XM_024453095.1:c.59510T>A
(TTN)
|
XP_024308863.1:p.Ile19837Asn
|
|
XM_024453096.1:c.58943T>A
(TTN)
|
XP_024308864.1:p.Ile19648Asn
|
|
XM_024453097.1:c.56285T>A
(TTN)
|
XP_024308865.1:p.Ile18762Asn
|
|
XM_024453098.1:c.56204T>A
(TTN)
|
XP_024308866.1:p.Ile18735Asn
|
|
XM_024453099.1:c.37967T>A
(TTN)
|
XP_024308867.1:p.Ile12656Asn
|
|
XM_024453100.1:c.27821T>A
(TTN)
|
XP_024308868.1:p.Ile9274Asn
|
|