ENST00000342992.11:c.88112C>A
(TTN)
|
ENSP00000343764.6:p.Thr29371Asn
|
|
ENST00000342175.11:c.69197C>A
(TTN)
|
ENSP00000340554.6:p.Thr23066Asn
|
|
ENST00000359218.10:c.68996C>A
(TTN)
|
ENSP00000352154.5:p.Thr22999Asn
|
|
ENST00000342175.10:c.69197C>A
(TTN)
|
ENSP00000340554.6:p.Thr23066Asn
|
|
ENST00000342992.10:c.88112C>A
(TTN)
|
ENSP00000343764.6:p.Thr29371Asn
|
|
ENST00000359218.9:c.68996C>A
(TTN)
|
ENSP00000352154.5:p.Thr22999Asn
|
|
ENST00000460472.6:c.68621C>A
(TTN)
|
ENSP00000434586.1:p.Thr22874Asn
|
|
ENST00000589042.5:c.95816C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31939Asn
|
|
ENST00000591111.5:c.90893C>A
(TTN)
|
ENSP00000465570.1:p.Thr30298Asn
|
|
ENST00000615779.4:c.90893C>A
(TTN)
|
ENSP00000483597.1:p.Thr30298Asn
|
|
NM_001256850.1:c.90893C>A
(TTN)
|
NP_001243779.1:p.Thr30298Asn
|
|
NM_001267550.2:c.95816C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31939Asn
|
|
NM_003319.4:c.68621C>A
(TTN)
|
NP_003310.4:p.Thr22874Asn
|
|
NM_133378.4:c.88112C>A
(TTN)
|
NP_596869.4:p.Thr29371Asn
|
|
NM_133432.3:c.68996C>A
(TTN)
|
NP_597676.3:p.Thr22999Asn
|
|
NM_133437.4:c.69197C>A
(TTN)
|
NP_597681.4:p.Thr23066Asn
|
|
NR_038271.1:n.446+20777G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2052G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.94913C>A
(TTN)
|
XP_011510031.1:p.Thr31638Asn
|
|
XM_011511730.1:c.68807C>A
(TTN)
|
XP_011510032.1:p.Thr22936Asn
|
|
XM_011511731.1:c.68666C>A
(TTN)
|
XP_011510033.1:p.Thr22889Asn
|
|
XM_017004819.1:c.94709C>A
(TTN)
|
XP_016860308.1:p.Thr31570Asn
|
|
XM_017004820.1:c.90107C>A
(TTN)
|
XP_016860309.1:p.Thr30036Asn
|
|
XM_017004821.1:c.90104C>A
(TTN)
|
XP_016860310.1:p.Thr30035Asn
|
|
XM_017004822.1:c.87146C>A
(TTN)
|
XP_016860311.1:p.Thr29049Asn
|
|
XM_017004823.1:c.68762C>A
(TTN)
|
XP_016860312.1:p.Thr22921Asn
|
|
XM_024453094.1:c.90257C>A
(TTN)
|
XP_024308862.1:p.Thr30086Asn
|
|
XM_024453095.1:c.90254C>A
(TTN)
|
XP_024308863.1:p.Thr30085Asn
|
|
XM_024453096.1:c.89687C>A
(TTN)
|
XP_024308864.1:p.Thr29896Asn
|
|
XM_024453097.1:c.87029C>A
(TTN)
|
XP_024308865.1:p.Thr29010Asn
|
|
XM_024453098.1:c.86948C>A
(TTN)
|
XP_024308866.1:p.Thr28983Asn
|
|
XM_024453099.1:c.68711C>A
(TTN)
|
XP_024308867.1:p.Thr22904Asn
|
|
XM_024453100.1:c.58565C>A
(TTN)
|
XP_024308868.1:p.Thr19522Asn
|
|