ENST00000342992.11:c.96671T>G
(TTN)
|
ENSP00000343764.6:p.Phe32224Cys
|
|
ENST00000342175.11:c.77756T>G
(TTN)
|
ENSP00000340554.6:p.Phe25919Cys
|
|
ENST00000359218.10:c.77555T>G
(TTN)
|
ENSP00000352154.5:p.Phe25852Cys
|
|
ENST00000342175.10:c.77756T>G
(TTN)
|
ENSP00000340554.6:p.Phe25919Cys
|
|
ENST00000342992.10:c.96671T>G
(TTN)
|
ENSP00000343764.6:p.Phe32224Cys
|
|
ENST00000359218.9:c.77555T>G
(TTN)
|
ENSP00000352154.5:p.Phe25852Cys
|
|
ENST00000460472.6:c.77180T>G
(TTN)
|
ENSP00000434586.1:p.Phe25727Cys
|
|
ENST00000589042.5:c.104375T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe34792Cys
|
|
ENST00000591111.5:c.99452T>G
(TTN)
|
ENSP00000465570.1:p.Phe33151Cys
|
|
ENST00000615779.4:c.99452T>G
(TTN)
|
ENSP00000483597.1:p.Phe33151Cys
|
|
NM_001256850.1:c.99452T>G
(TTN)
|
NP_001243779.1:p.Phe33151Cys
|
|
NM_001267550.2:c.104375T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Phe34792Cys
|
|
NM_003319.4:c.77180T>G
(TTN)
|
NP_003310.4:p.Phe25727Cys
|
|
NM_133378.4:c.96671T>G
(TTN)
|
NP_596869.4:p.Phe32224Cys
|
|
NM_133432.3:c.77555T>G
(TTN)
|
NP_597676.3:p.Phe25852Cys
|
|
NM_133437.4:c.77756T>G
(TTN)
|
NP_597681.4:p.Phe25919Cys
|
|
NR_038271.1:n.446+8604A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3492A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103472T>G
(TTN)
|
XP_011510031.1:p.Phe34491Cys
|
|
XM_011511730.1:c.77366T>G
(TTN)
|
XP_011510032.1:p.Phe25789Cys
|
|
XM_011511731.1:c.77225T>G
(TTN)
|
XP_011510033.1:p.Phe25742Cys
|
|
XM_017004819.1:c.103268T>G
(TTN)
|
XP_016860308.1:p.Phe34423Cys
|
|
XM_017004820.1:c.98666T>G
(TTN)
|
XP_016860309.1:p.Phe32889Cys
|
|
XM_017004821.1:c.98663T>G
(TTN)
|
XP_016860310.1:p.Phe32888Cys
|
|
XM_017004822.1:c.95705T>G
(TTN)
|
XP_016860311.1:p.Phe31902Cys
|
|
XM_017004823.1:c.77321T>G
(TTN)
|
XP_016860312.1:p.Phe25774Cys
|
|
XM_024453094.1:c.98816T>G
(TTN)
|
XP_024308862.1:p.Phe32939Cys
|
|
XM_024453095.1:c.98813T>G
(TTN)
|
XP_024308863.1:p.Phe32938Cys
|
|
XM_024453096.1:c.98246T>G
(TTN)
|
XP_024308864.1:p.Phe32749Cys
|
|
XM_024453097.1:c.95588T>G
(TTN)
|
XP_024308865.1:p.Phe31863Cys
|
|
XM_024453098.1:c.95507T>G
(TTN)
|
XP_024308866.1:p.Phe31836Cys
|
|
XM_024453099.1:c.77270T>G
(TTN)
|
XP_024308867.1:p.Phe25757Cys
|
|
XM_024453100.1:c.67124T>G
(TTN)
|
XP_024308868.1:p.Phe22375Cys
|
|