ENST00000342992.11:c.64562A>C
(TTN)
|
ENSP00000343764.6:p.Asn21521Thr
|
|
ENST00000342175.11:c.45647A>C
(TTN)
|
ENSP00000340554.6:p.Asn15216Thr
|
|
ENST00000359218.10:c.45446A>C
(TTN)
|
ENSP00000352154.5:p.Asn15149Thr
|
|
ENST00000342175.10:c.45647A>C
(TTN)
|
ENSP00000340554.6:p.Asn15216Thr
|
|
ENST00000342992.10:c.64562A>C
(TTN)
|
ENSP00000343764.6:p.Asn21521Thr
|
|
ENST00000359218.9:c.45446A>C
(TTN)
|
ENSP00000352154.5:p.Asn15149Thr
|
|
ENST00000460472.6:c.45071A>C
(TTN)
|
ENSP00000434586.1:p.Asn15024Thr
|
|
ENST00000589042.5:c.72266A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn24089Thr
|
|
ENST00000591111.5:c.67343A>C
(TTN)
|
ENSP00000465570.1:p.Asn22448Thr
|
|
ENST00000615779.4:c.67343A>C
(TTN)
|
ENSP00000483597.1:p.Asn22448Thr
|
|
NM_001256850.1:c.67343A>C
(TTN)
|
NP_001243779.1:p.Asn22448Thr
|
|
NM_001267550.2:c.72266A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asn24089Thr
|
|
NM_003319.4:c.45071A>C
(TTN)
|
NP_003310.4:p.Asn15024Thr
|
|
NM_133378.4:c.64562A>C
(TTN)
|
NP_596869.4:p.Asn21521Thr
|
|
NM_133432.3:c.45446A>C
(TTN)
|
NP_597676.3:p.Asn15149Thr
|
|
NM_133437.4:c.45647A>C
(TTN)
|
NP_597681.4:p.Asn15216Thr
|
|
NR_038271.1:n.596+2417T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-8706T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.71363A>C
(TTN)
|
XP_011510031.1:p.Asn23788Thr
|
|
XM_011511730.1:c.45257A>C
(TTN)
|
XP_011510032.1:p.Asn15086Thr
|
|
XM_011511731.1:c.45116A>C
(TTN)
|
XP_011510033.1:p.Asn15039Thr
|
|
XM_017004819.1:c.71159A>C
(TTN)
|
XP_016860308.1:p.Asn23720Thr
|
|
XM_017004820.1:c.66557A>C
(TTN)
|
XP_016860309.1:p.Asn22186Thr
|
|
XM_017004821.1:c.66554A>C
(TTN)
|
XP_016860310.1:p.Asn22185Thr
|
|
XM_017004822.1:c.63596A>C
(TTN)
|
XP_016860311.1:p.Asn21199Thr
|
|
XM_017004823.1:c.45212A>C
(TTN)
|
XP_016860312.1:p.Asn15071Thr
|
|
XM_024453094.1:c.66707A>C
(TTN)
|
XP_024308862.1:p.Asn22236Thr
|
|
XM_024453095.1:c.66704A>C
(TTN)
|
XP_024308863.1:p.Asn22235Thr
|
|
XM_024453096.1:c.66137A>C
(TTN)
|
XP_024308864.1:p.Asn22046Thr
|
|
XM_024453097.1:c.63479A>C
(TTN)
|
XP_024308865.1:p.Asn21160Thr
|
|
XM_024453098.1:c.63398A>C
(TTN)
|
XP_024308866.1:p.Asn21133Thr
|
|
XM_024453099.1:c.45161A>C
(TTN)
|
XP_024308867.1:p.Asn15054Thr
|
|
XM_024453100.1:c.35015A>C
(TTN)
|
XP_024308868.1:p.Asn11672Thr
|
|