ENST00000342992.11:c.88112C>G
(TTN)
|
ENSP00000343764.6:p.Thr29371Ser
|
|
ENST00000342175.11:c.69197C>G
(TTN)
|
ENSP00000340554.6:p.Thr23066Ser
|
|
ENST00000359218.10:c.68996C>G
(TTN)
|
ENSP00000352154.5:p.Thr22999Ser
|
|
ENST00000342175.10:c.69197C>G
(TTN)
|
ENSP00000340554.6:p.Thr23066Ser
|
|
ENST00000342992.10:c.88112C>G
(TTN)
|
ENSP00000343764.6:p.Thr29371Ser
|
|
ENST00000359218.9:c.68996C>G
(TTN)
|
ENSP00000352154.5:p.Thr22999Ser
|
|
ENST00000460472.6:c.68621C>G
(TTN)
|
ENSP00000434586.1:p.Thr22874Ser
|
|
ENST00000589042.5:c.95816C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31939Ser
|
|
ENST00000591111.5:c.90893C>G
(TTN)
|
ENSP00000465570.1:p.Thr30298Ser
|
|
ENST00000615779.4:c.90893C>G
(TTN)
|
ENSP00000483597.1:p.Thr30298Ser
|
|
NM_001256850.1:c.90893C>G
(TTN)
|
NP_001243779.1:p.Thr30298Ser
|
|
NM_001267550.2:c.95816C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31939Ser
|
|
NM_003319.4:c.68621C>G
(TTN)
|
NP_003310.4:p.Thr22874Ser
|
|
NM_133378.4:c.88112C>G
(TTN)
|
NP_596869.4:p.Thr29371Ser
|
|
NM_133432.3:c.68996C>G
(TTN)
|
NP_597676.3:p.Thr22999Ser
|
|
NM_133437.4:c.69197C>G
(TTN)
|
NP_597681.4:p.Thr23066Ser
|
|
NR_038271.1:n.446+20777G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2052G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.94913C>G
(TTN)
|
XP_011510031.1:p.Thr31638Ser
|
|
XM_011511730.1:c.68807C>G
(TTN)
|
XP_011510032.1:p.Thr22936Ser
|
|
XM_011511731.1:c.68666C>G
(TTN)
|
XP_011510033.1:p.Thr22889Ser
|
|
XM_017004819.1:c.94709C>G
(TTN)
|
XP_016860308.1:p.Thr31570Ser
|
|
XM_017004820.1:c.90107C>G
(TTN)
|
XP_016860309.1:p.Thr30036Ser
|
|
XM_017004821.1:c.90104C>G
(TTN)
|
XP_016860310.1:p.Thr30035Ser
|
|
XM_017004822.1:c.87146C>G
(TTN)
|
XP_016860311.1:p.Thr29049Ser
|
|
XM_017004823.1:c.68762C>G
(TTN)
|
XP_016860312.1:p.Thr22921Ser
|
|
XM_024453094.1:c.90257C>G
(TTN)
|
XP_024308862.1:p.Thr30086Ser
|
|
XM_024453095.1:c.90254C>G
(TTN)
|
XP_024308863.1:p.Thr30085Ser
|
|
XM_024453096.1:c.89687C>G
(TTN)
|
XP_024308864.1:p.Thr29896Ser
|
|
XM_024453097.1:c.87029C>G
(TTN)
|
XP_024308865.1:p.Thr29010Ser
|
|
XM_024453098.1:c.86948C>G
(TTN)
|
XP_024308866.1:p.Thr28983Ser
|
|
XM_024453099.1:c.68711C>G
(TTN)
|
XP_024308867.1:p.Thr22904Ser
|
|
XM_024453100.1:c.58565C>G
(TTN)
|
XP_024308868.1:p.Thr19522Ser
|
|