ENST00000342992.11:c.39166A>G
(TTN)
|
ENSP00000343764.6:p.Ile13056Val
|
|
ENST00000342175.11:c.20251A>G
(TTN)
|
ENSP00000340554.6:p.Ile6751Val
|
|
ENST00000359218.10:c.20050A>G
(TTN)
|
ENSP00000352154.5:p.Ile6684Val
|
|
ENST00000342175.10:c.20251A>G
(TTN)
|
ENSP00000340554.6:p.Ile6751Val
|
|
ENST00000342992.10:c.39166A>G
(TTN)
|
ENSP00000343764.6:p.Ile13056Val
|
|
ENST00000359218.9:c.20050A>G
(TTN)
|
ENSP00000352154.5:p.Ile6684Val
|
|
ENST00000460472.6:c.19675A>G
(TTN)
|
ENSP00000434586.1:p.Ile6559Val
|
|
ENST00000589042.5:c.46870A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile15624Val
|
|
ENST00000591111.5:c.41947A>G
(TTN)
|
ENSP00000465570.1:p.Ile13983Val
|
|
ENST00000615779.4:c.41947A>G
(TTN)
|
ENSP00000483597.1:p.Ile13983Val
|
|
NM_001256850.1:c.41947A>G
(TTN)
|
NP_001243779.1:p.Ile13983Val
|
|
NM_001267550.2:c.46870A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ile15624Val
|
|
NM_003319.4:c.19675A>G
(TTN)
|
NP_003310.4:p.Ile6559Val
|
|
NM_133378.4:c.39166A>G
(TTN)
|
NP_596869.4:p.Ile13056Val
|
|
NM_133432.3:c.20050A>G
(TTN)
|
NP_597676.3:p.Ile6684Val
|
|
NM_133437.4:c.20251A>G
(TTN)
|
NP_597681.4:p.Ile6751Val
|
|
NR_038271.1:n.1605-1073T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.45967A>G
(TTN)
|
XP_011510031.1:p.Ile15323Val
|
|
XM_011511730.1:c.19861A>G
(TTN)
|
XP_011510032.1:p.Ile6621Val
|
|
XM_011511731.1:c.19720A>G
(TTN)
|
XP_011510033.1:p.Ile6574Val
|
|
XM_017004819.1:c.45763A>G
(TTN)
|
XP_016860308.1:p.Ile15255Val
|
|
XM_017004820.1:c.41161A>G
(TTN)
|
XP_016860309.1:p.Ile13721Val
|
|
XM_017004821.1:c.41158A>G
(TTN)
|
XP_016860310.1:p.Ile13720Val
|
|
XM_017004822.1:c.38200A>G
(TTN)
|
XP_016860311.1:p.Ile12734Val
|
|
XM_017004823.1:c.19816A>G
(TTN)
|
XP_016860312.1:p.Ile6606Val
|
|
XM_024453094.1:c.41311A>G
(TTN)
|
XP_024308862.1:p.Ile13771Val
|
|
XM_024453095.1:c.41308A>G
(TTN)
|
XP_024308863.1:p.Ile13770Val
|
|
XM_024453096.1:c.40741A>G
(TTN)
|
XP_024308864.1:p.Ile13581Val
|
|
XM_024453097.1:c.38083A>G
(TTN)
|
XP_024308865.1:p.Ile12695Val
|
|
XM_024453098.1:c.38002A>G
(TTN)
|
XP_024308866.1:p.Ile12668Val
|
|
XM_024453099.1:c.19765A>G
(TTN)
|
XP_024308867.1:p.Ile6589Val
|
|
XM_024453100.1:c.9619A>G
(TTN)
|
XP_024308868.1:p.Ile3207Val
|
|