ENST00000342992.11:c.98741C>A
(TTN)
|
ENSP00000343764.6:p.Thr32914Asn
|
|
ENST00000342175.11:c.79826C>A
(TTN)
|
ENSP00000340554.6:p.Thr26609Asn
|
|
ENST00000359218.10:c.79625C>A
(TTN)
|
ENSP00000352154.5:p.Thr26542Asn
|
|
ENST00000342175.10:c.79826C>A
(TTN)
|
ENSP00000340554.6:p.Thr26609Asn
|
|
ENST00000342992.10:c.98741C>A
(TTN)
|
ENSP00000343764.6:p.Thr32914Asn
|
|
ENST00000359218.9:c.79625C>A
(TTN)
|
ENSP00000352154.5:p.Thr26542Asn
|
|
ENST00000460472.6:c.79250C>A
(TTN)
|
ENSP00000434586.1:p.Thr26417Asn
|
|
ENST00000589042.5:c.106445C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35482Asn
|
|
ENST00000591111.5:c.101522C>A
(TTN)
|
ENSP00000465570.1:p.Thr33841Asn
|
|
ENST00000615779.4:c.101522C>A
(TTN)
|
ENSP00000483597.1:p.Thr33841Asn
|
|
NM_001256850.1:c.101522C>A
(TTN)
|
NP_001243779.1:p.Thr33841Asn
|
|
NM_001267550.2:c.106445C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35482Asn
|
|
NM_003319.4:c.79250C>A
(TTN)
|
NP_003310.4:p.Thr26417Asn
|
|
NM_133378.4:c.98741C>A
(TTN)
|
NP_596869.4:p.Thr32914Asn
|
|
NM_133432.3:c.79625C>A
(TTN)
|
NP_597676.3:p.Thr26542Asn
|
|
NM_133437.4:c.79826C>A
(TTN)
|
NP_597681.4:p.Thr26609Asn
|
|
NR_038271.1:n.446+6410G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5686G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105542C>A
(TTN)
|
XP_011510031.1:p.Thr35181Asn
|
|
XM_011511730.1:c.79436C>A
(TTN)
|
XP_011510032.1:p.Thr26479Asn
|
|
XM_011511731.1:c.79295C>A
(TTN)
|
XP_011510033.1:p.Thr26432Asn
|
|
XM_017004819.1:c.105338C>A
(TTN)
|
XP_016860308.1:p.Thr35113Asn
|
|
XM_017004820.1:c.100736C>A
(TTN)
|
XP_016860309.1:p.Thr33579Asn
|
|
XM_017004821.1:c.100733C>A
(TTN)
|
XP_016860310.1:p.Thr33578Asn
|
|
XM_017004822.1:c.97775C>A
(TTN)
|
XP_016860311.1:p.Thr32592Asn
|
|
XM_017004823.1:c.79391C>A
(TTN)
|
XP_016860312.1:p.Thr26464Asn
|
|
XM_024453094.1:c.100886C>A
(TTN)
|
XP_024308862.1:p.Thr33629Asn
|
|
XM_024453095.1:c.100883C>A
(TTN)
|
XP_024308863.1:p.Thr33628Asn
|
|
XM_024453096.1:c.100316C>A
(TTN)
|
XP_024308864.1:p.Thr33439Asn
|
|
XM_024453097.1:c.97658C>A
(TTN)
|
XP_024308865.1:p.Thr32553Asn
|
|
XM_024453098.1:c.97577C>A
(TTN)
|
XP_024308866.1:p.Thr32526Asn
|
|
XM_024453099.1:c.79340C>A
(TTN)
|
XP_024308867.1:p.Thr26447Asn
|
|
XM_024453100.1:c.69194C>A
(TTN)
|
XP_024308868.1:p.Thr23065Asn
|
|