ENST00000342992.11:c.51358G>A
(TTN)
|
ENSP00000343764.6:p.Glu17120Lys
|
|
ENST00000342175.11:c.32443G>A
(TTN)
|
ENSP00000340554.6:p.Glu10815Lys
|
|
ENST00000359218.10:c.32242G>A
(TTN)
|
ENSP00000352154.5:p.Glu10748Lys
|
|
ENST00000342175.10:c.32443G>A
(TTN)
|
ENSP00000340554.6:p.Glu10815Lys
|
|
ENST00000342992.10:c.51358G>A
(TTN)
|
ENSP00000343764.6:p.Glu17120Lys
|
|
ENST00000359218.9:c.32242G>A
(TTN)
|
ENSP00000352154.5:p.Glu10748Lys
|
|
ENST00000460472.6:c.31867G>A
(TTN)
|
ENSP00000434586.1:p.Glu10623Lys
|
|
ENST00000589042.5:c.59062G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu19688Lys
|
|
ENST00000591111.5:c.54139G>A
(TTN)
|
ENSP00000465570.1:p.Glu18047Lys
|
|
ENST00000615779.4:c.54139G>A
(TTN)
|
ENSP00000483597.1:p.Glu18047Lys
|
|
NM_001256850.1:c.54139G>A
(TTN)
|
NP_001243779.1:p.Glu18047Lys
|
|
NM_001267550.2:c.59062G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Glu19688Lys
|
|
NM_003319.4:c.31867G>A
(TTN)
|
NP_003310.4:p.Glu10623Lys
|
|
NM_133378.4:c.51358G>A
(TTN)
|
NP_596869.4:p.Glu17120Lys
|
|
NM_133432.3:c.32242G>A
(TTN)
|
NP_597676.3:p.Glu10748Lys
|
|
NM_133437.4:c.32443G>A
(TTN)
|
NP_597681.4:p.Glu10815Lys
|
|
NR_038271.1:n.597-4539C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1743C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.58159G>A
(TTN)
|
XP_011510031.1:p.Glu19387Lys
|
|
XM_011511730.1:c.32053G>A
(TTN)
|
XP_011510032.1:p.Glu10685Lys
|
|
XM_011511731.1:c.31912G>A
(TTN)
|
XP_011510033.1:p.Glu10638Lys
|
|
XM_017004819.1:c.57955G>A
(TTN)
|
XP_016860308.1:p.Glu19319Lys
|
|
XM_017004820.1:c.53353G>A
(TTN)
|
XP_016860309.1:p.Glu17785Lys
|
|
XM_017004821.1:c.53350G>A
(TTN)
|
XP_016860310.1:p.Glu17784Lys
|
|
XM_017004822.1:c.50392G>A
(TTN)
|
XP_016860311.1:p.Glu16798Lys
|
|
XM_017004823.1:c.32008G>A
(TTN)
|
XP_016860312.1:p.Glu10670Lys
|
|
XM_024453094.1:c.53503G>A
(TTN)
|
XP_024308862.1:p.Glu17835Lys
|
|
XM_024453095.1:c.53500G>A
(TTN)
|
XP_024308863.1:p.Glu17834Lys
|
|
XM_024453096.1:c.52933G>A
(TTN)
|
XP_024308864.1:p.Glu17645Lys
|
|
XM_024453097.1:c.50275G>A
(TTN)
|
XP_024308865.1:p.Glu16759Lys
|
|
XM_024453098.1:c.50194G>A
(TTN)
|
XP_024308866.1:p.Glu16732Lys
|
|
XM_024453099.1:c.31957G>A
(TTN)
|
XP_024308867.1:p.Glu10653Lys
|
|
XM_024453100.1:c.21811G>A
(TTN)
|
XP_024308868.1:p.Glu7271Lys
|
|