ENST00000342992.11:c.98505A>C
(TTN)
|
ENSP00000343764.6:p.Thr32835=
|
|
ENST00000342175.11:c.79590A>C
(TTN)
|
ENSP00000340554.6:p.Thr26530=
|
|
ENST00000359218.10:c.79389A>C
(TTN)
|
ENSP00000352154.5:p.Thr26463=
|
|
ENST00000342175.10:c.79590A>C
(TTN)
|
ENSP00000340554.6:p.Thr26530=
|
|
ENST00000342992.10:c.98505A>C
(TTN)
|
ENSP00000343764.6:p.Thr32835=
|
|
ENST00000359218.9:c.79389A>C
(TTN)
|
ENSP00000352154.5:p.Thr26463=
|
|
ENST00000460472.6:c.79014A>C
(TTN)
|
ENSP00000434586.1:p.Thr26338=
|
|
ENST00000589042.5:c.106209A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35403=
|
|
ENST00000591111.5:c.101286A>C
(TTN)
|
ENSP00000465570.1:p.Thr33762=
|
|
ENST00000615779.4:c.101286A>C
(TTN)
|
ENSP00000483597.1:p.Thr33762=
|
|
NM_001256850.1:c.101286A>C
(TTN)
|
NP_001243779.1:p.Thr33762=
|
|
NM_001267550.2:c.106209A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35403=
|
|
NM_003319.4:c.79014A>C
(TTN)
|
NP_003310.4:p.Thr26338=
|
|
NM_133378.4:c.98505A>C
(TTN)
|
NP_596869.4:p.Thr32835=
|
|
NM_133432.3:c.79389A>C
(TTN)
|
NP_597676.3:p.Thr26463=
|
|
NM_133437.4:c.79590A>C
(TTN)
|
NP_597681.4:p.Thr26530=
|
|
NR_038271.1:n.446+6770T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5326T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105306A>C
(TTN)
|
XP_011510031.1:p.Thr35102=
|
|
XM_011511730.1:c.79200A>C
(TTN)
|
XP_011510032.1:p.Thr26400=
|
|
XM_011511731.1:c.79059A>C
(TTN)
|
XP_011510033.1:p.Thr26353=
|
|
XM_017004819.1:c.105102A>C
(TTN)
|
XP_016860308.1:p.Thr35034=
|
|
XM_017004820.1:c.100500A>C
(TTN)
|
XP_016860309.1:p.Thr33500=
|
|
XM_017004821.1:c.100497A>C
(TTN)
|
XP_016860310.1:p.Thr33499=
|
|
XM_017004822.1:c.97539A>C
(TTN)
|
XP_016860311.1:p.Thr32513=
|
|
XM_017004823.1:c.79155A>C
(TTN)
|
XP_016860312.1:p.Thr26385=
|
|
XM_024453094.1:c.100650A>C
(TTN)
|
XP_024308862.1:p.Thr33550=
|
|
XM_024453095.1:c.100647A>C
(TTN)
|
XP_024308863.1:p.Thr33549=
|
|
XM_024453096.1:c.100080A>C
(TTN)
|
XP_024308864.1:p.Thr33360=
|
|
XM_024453097.1:c.97422A>C
(TTN)
|
XP_024308865.1:p.Thr32474=
|
|
XM_024453098.1:c.97341A>C
(TTN)
|
XP_024308866.1:p.Thr32447=
|
|
XM_024453099.1:c.79104A>C
(TTN)
|
XP_024308867.1:p.Thr26368=
|
|
XM_024453100.1:c.68958A>C
(TTN)
|
XP_024308868.1:p.Thr22986=
|
|