ENST00000342992.11:c.96650A>C
(TTN)
|
ENSP00000343764.6:p.Glu32217Ala
|
|
ENST00000342175.11:c.77735A>C
(TTN)
|
ENSP00000340554.6:p.Glu25912Ala
|
|
ENST00000359218.10:c.77534A>C
(TTN)
|
ENSP00000352154.5:p.Glu25845Ala
|
|
ENST00000342175.10:c.77735A>C
(TTN)
|
ENSP00000340554.6:p.Glu25912Ala
|
|
ENST00000342992.10:c.96650A>C
(TTN)
|
ENSP00000343764.6:p.Glu32217Ala
|
|
ENST00000359218.9:c.77534A>C
(TTN)
|
ENSP00000352154.5:p.Glu25845Ala
|
|
ENST00000460472.6:c.77159A>C
(TTN)
|
ENSP00000434586.1:p.Glu25720Ala
|
|
ENST00000589042.5:c.104354A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34785Ala
|
|
ENST00000591111.5:c.99431A>C
(TTN)
|
ENSP00000465570.1:p.Glu33144Ala
|
|
ENST00000615779.4:c.99431A>C
(TTN)
|
ENSP00000483597.1:p.Glu33144Ala
|
|
NM_001256850.1:c.99431A>C
(TTN)
|
NP_001243779.1:p.Glu33144Ala
|
|
NM_001267550.2:c.104354A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34785Ala
|
|
NM_003319.4:c.77159A>C
(TTN)
|
NP_003310.4:p.Glu25720Ala
|
|
NM_133378.4:c.96650A>C
(TTN)
|
NP_596869.4:p.Glu32217Ala
|
|
NM_133432.3:c.77534A>C
(TTN)
|
NP_597676.3:p.Glu25845Ala
|
|
NM_133437.4:c.77735A>C
(TTN)
|
NP_597681.4:p.Glu25912Ala
|
|
NR_038271.1:n.446+8625T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3471T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103451A>C
(TTN)
|
XP_011510031.1:p.Glu34484Ala
|
|
XM_011511730.1:c.77345A>C
(TTN)
|
XP_011510032.1:p.Glu25782Ala
|
|
XM_011511731.1:c.77204A>C
(TTN)
|
XP_011510033.1:p.Glu25735Ala
|
|
XM_017004819.1:c.103247A>C
(TTN)
|
XP_016860308.1:p.Glu34416Ala
|
|
XM_017004820.1:c.98645A>C
(TTN)
|
XP_016860309.1:p.Glu32882Ala
|
|
XM_017004821.1:c.98642A>C
(TTN)
|
XP_016860310.1:p.Glu32881Ala
|
|
XM_017004822.1:c.95684A>C
(TTN)
|
XP_016860311.1:p.Glu31895Ala
|
|
XM_017004823.1:c.77300A>C
(TTN)
|
XP_016860312.1:p.Glu25767Ala
|
|
XM_024453094.1:c.98795A>C
(TTN)
|
XP_024308862.1:p.Glu32932Ala
|
|
XM_024453095.1:c.98792A>C
(TTN)
|
XP_024308863.1:p.Glu32931Ala
|
|
XM_024453096.1:c.98225A>C
(TTN)
|
XP_024308864.1:p.Glu32742Ala
|
|
XM_024453097.1:c.95567A>C
(TTN)
|
XP_024308865.1:p.Glu31856Ala
|
|
XM_024453098.1:c.95486A>C
(TTN)
|
XP_024308866.1:p.Glu31829Ala
|
|
XM_024453099.1:c.77249A>C
(TTN)
|
XP_024308867.1:p.Glu25750Ala
|
|
XM_024453100.1:c.67103A>C
(TTN)
|
XP_024308868.1:p.Glu22368Ala
|
|