ENST00000342992.11:c.50665T>A
(TTN)
|
ENSP00000343764.6:p.Tyr16889Asn
|
|
ENST00000342175.11:c.31750T>A
(TTN)
|
ENSP00000340554.6:p.Tyr10584Asn
|
|
ENST00000359218.10:c.31549T>A
(TTN)
|
ENSP00000352154.5:p.Tyr10517Asn
|
|
ENST00000342175.10:c.31750T>A
(TTN)
|
ENSP00000340554.6:p.Tyr10584Asn
|
|
ENST00000342992.10:c.50665T>A
(TTN)
|
ENSP00000343764.6:p.Tyr16889Asn
|
|
ENST00000359218.9:c.31549T>A
(TTN)
|
ENSP00000352154.5:p.Tyr10517Asn
|
|
ENST00000460472.6:c.31174T>A
(TTN)
|
ENSP00000434586.1:p.Tyr10392Asn
|
|
ENST00000589042.5:c.58369T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr19457Asn
|
|
ENST00000591111.5:c.53446T>A
(TTN)
|
ENSP00000465570.1:p.Tyr17816Asn
|
|
ENST00000615779.4:c.53446T>A
(TTN)
|
ENSP00000483597.1:p.Tyr17816Asn
|
|
NM_001256850.1:c.53446T>A
(TTN)
|
NP_001243779.1:p.Tyr17816Asn
|
|
NM_001267550.2:c.58369T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr19457Asn
|
|
NM_003319.4:c.31174T>A
(TTN)
|
NP_003310.4:p.Tyr10392Asn
|
|
NM_133378.4:c.50665T>A
(TTN)
|
NP_596869.4:p.Tyr16889Asn
|
|
NM_133432.3:c.31549T>A
(TTN)
|
NP_597676.3:p.Tyr10517Asn
|
|
NM_133437.4:c.31750T>A
(TTN)
|
NP_597681.4:p.Tyr10584Asn
|
|
NR_038271.1:n.597-3572A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+2710A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.57466T>A
(TTN)
|
XP_011510031.1:p.Tyr19156Asn
|
|
XM_011511730.1:c.31360T>A
(TTN)
|
XP_011510032.1:p.Tyr10454Asn
|
|
XM_011511731.1:c.31219T>A
(TTN)
|
XP_011510033.1:p.Tyr10407Asn
|
|
XM_017004819.1:c.57262T>A
(TTN)
|
XP_016860308.1:p.Tyr19088Asn
|
|
XM_017004820.1:c.52660T>A
(TTN)
|
XP_016860309.1:p.Tyr17554Asn
|
|
XM_017004821.1:c.52657T>A
(TTN)
|
XP_016860310.1:p.Tyr17553Asn
|
|
XM_017004822.1:c.49699T>A
(TTN)
|
XP_016860311.1:p.Tyr16567Asn
|
|
XM_017004823.1:c.31315T>A
(TTN)
|
XP_016860312.1:p.Tyr10439Asn
|
|
XM_024453094.1:c.52810T>A
(TTN)
|
XP_024308862.1:p.Tyr17604Asn
|
|
XM_024453095.1:c.52807T>A
(TTN)
|
XP_024308863.1:p.Tyr17603Asn
|
|
XM_024453096.1:c.52240T>A
(TTN)
|
XP_024308864.1:p.Tyr17414Asn
|
|
XM_024453097.1:c.49582T>A
(TTN)
|
XP_024308865.1:p.Tyr16528Asn
|
|
XM_024453098.1:c.49501T>A
(TTN)
|
XP_024308866.1:p.Tyr16501Asn
|
|
XM_024453099.1:c.31264T>A
(TTN)
|
XP_024308867.1:p.Tyr10422Asn
|
|
XM_024453100.1:c.21118T>A
(TTN)
|
XP_024308868.1:p.Tyr7040Asn
|
|