ENST00000342992.11:c.51354T>C
(TTN)
|
ENSP00000343764.6:p.Asn17118=
|
|
ENST00000342175.11:c.32439T>C
(TTN)
|
ENSP00000340554.6:p.Asn10813=
|
|
ENST00000359218.10:c.32238T>C
(TTN)
|
ENSP00000352154.5:p.Asn10746=
|
|
ENST00000342175.10:c.32439T>C
(TTN)
|
ENSP00000340554.6:p.Asn10813=
|
|
ENST00000342992.10:c.51354T>C
(TTN)
|
ENSP00000343764.6:p.Asn17118=
|
|
ENST00000359218.9:c.32238T>C
(TTN)
|
ENSP00000352154.5:p.Asn10746=
|
|
ENST00000460472.6:c.31863T>C
(TTN)
|
ENSP00000434586.1:p.Asn10621=
|
|
ENST00000589042.5:c.59058T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn19686=
|
|
ENST00000591111.5:c.54135T>C
(TTN)
|
ENSP00000465570.1:p.Asn18045=
|
|
ENST00000615779.4:c.54135T>C
(TTN)
|
ENSP00000483597.1:p.Asn18045=
|
|
NM_001256850.1:c.54135T>C
(TTN)
|
NP_001243779.1:p.Asn18045=
|
|
NM_001267550.2:c.59058T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asn19686=
|
|
NM_003319.4:c.31863T>C
(TTN)
|
NP_003310.4:p.Asn10621=
|
|
NM_133378.4:c.51354T>C
(TTN)
|
NP_596869.4:p.Asn17118=
|
|
NM_133432.3:c.32238T>C
(TTN)
|
NP_597676.3:p.Asn10746=
|
|
NM_133437.4:c.32439T>C
(TTN)
|
NP_597681.4:p.Asn10813=
|
|
NR_038271.1:n.597-4535A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1747A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.58155T>C
(TTN)
|
XP_011510031.1:p.Asn19385=
|
|
XM_011511730.1:c.32049T>C
(TTN)
|
XP_011510032.1:p.Asn10683=
|
|
XM_011511731.1:c.31908T>C
(TTN)
|
XP_011510033.1:p.Asn10636=
|
|
XM_017004819.1:c.57951T>C
(TTN)
|
XP_016860308.1:p.Asn19317=
|
|
XM_017004820.1:c.53349T>C
(TTN)
|
XP_016860309.1:p.Asn17783=
|
|
XM_017004821.1:c.53346T>C
(TTN)
|
XP_016860310.1:p.Asn17782=
|
|
XM_017004822.1:c.50388T>C
(TTN)
|
XP_016860311.1:p.Asn16796=
|
|
XM_017004823.1:c.32004T>C
(TTN)
|
XP_016860312.1:p.Asn10668=
|
|
XM_024453094.1:c.53499T>C
(TTN)
|
XP_024308862.1:p.Asn17833=
|
|
XM_024453095.1:c.53496T>C
(TTN)
|
XP_024308863.1:p.Asn17832=
|
|
XM_024453096.1:c.52929T>C
(TTN)
|
XP_024308864.1:p.Asn17643=
|
|
XM_024453097.1:c.50271T>C
(TTN)
|
XP_024308865.1:p.Asn16757=
|
|
XM_024453098.1:c.50190T>C
(TTN)
|
XP_024308866.1:p.Asn16730=
|
|
XM_024453099.1:c.31953T>C
(TTN)
|
XP_024308867.1:p.Asn10651=
|
|
XM_024453100.1:c.21807T>C
(TTN)
|
XP_024308868.1:p.Asn7269=
|
|