ENST00000342992.11:c.69504A>T
(TTN)
|
ENSP00000343764.6:p.Glu23168Asp
|
|
ENST00000342175.11:c.50589A>T
(TTN)
|
ENSP00000340554.6:p.Glu16863Asp
|
|
ENST00000359218.10:c.50388A>T
(TTN)
|
ENSP00000352154.5:p.Glu16796Asp
|
|
ENST00000342175.10:c.50589A>T
(TTN)
|
ENSP00000340554.6:p.Glu16863Asp
|
|
ENST00000342992.10:c.69504A>T
(TTN)
|
ENSP00000343764.6:p.Glu23168Asp
|
|
ENST00000359218.9:c.50388A>T
(TTN)
|
ENSP00000352154.5:p.Glu16796Asp
|
|
ENST00000460472.6:c.50013A>T
(TTN)
|
ENSP00000434586.1:p.Glu16671Asp
|
|
ENST00000589042.5:c.77208A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu25736Asp
|
|
ENST00000591111.5:c.72285A>T
(TTN)
|
ENSP00000465570.1:p.Glu24095Asp
|
|
ENST00000615779.4:c.72285A>T
(TTN)
|
ENSP00000483597.1:p.Glu24095Asp
|
|
NM_001256850.1:c.72285A>T
(TTN)
|
NP_001243779.1:p.Glu24095Asp
|
|
NM_001267550.2:c.77208A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu25736Asp
|
|
NM_003319.4:c.50013A>T
(TTN)
|
NP_003310.4:p.Glu16671Asp
|
|
NM_133378.4:c.69504A>T
(TTN)
|
NP_596869.4:p.Glu23168Asp
|
|
NM_133432.3:c.50388A>T
(TTN)
|
NP_597676.3:p.Glu16796Asp
|
|
NM_133437.4:c.50589A>T
(TTN)
|
NP_597681.4:p.Glu16863Asp
|
|
NR_038271.1:n.447-2376T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13648T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.76305A>T
(TTN)
|
XP_011510031.1:p.Glu25435Asp
|
|
XM_011511730.1:c.50199A>T
(TTN)
|
XP_011510032.1:p.Glu16733Asp
|
|
XM_011511731.1:c.50058A>T
(TTN)
|
XP_011510033.1:p.Glu16686Asp
|
|
XM_017004819.1:c.76101A>T
(TTN)
|
XP_016860308.1:p.Glu25367Asp
|
|
XM_017004820.1:c.71499A>T
(TTN)
|
XP_016860309.1:p.Glu23833Asp
|
|
XM_017004821.1:c.71496A>T
(TTN)
|
XP_016860310.1:p.Glu23832Asp
|
|
XM_017004822.1:c.68538A>T
(TTN)
|
XP_016860311.1:p.Glu22846Asp
|
|
XM_017004823.1:c.50154A>T
(TTN)
|
XP_016860312.1:p.Glu16718Asp
|
|
XM_024453094.1:c.71649A>T
(TTN)
|
XP_024308862.1:p.Glu23883Asp
|
|
XM_024453095.1:c.71646A>T
(TTN)
|
XP_024308863.1:p.Glu23882Asp
|
|
XM_024453096.1:c.71079A>T
(TTN)
|
XP_024308864.1:p.Glu23693Asp
|
|
XM_024453097.1:c.68421A>T
(TTN)
|
XP_024308865.1:p.Glu22807Asp
|
|
XM_024453098.1:c.68340A>T
(TTN)
|
XP_024308866.1:p.Glu22780Asp
|
|
XM_024453099.1:c.50103A>T
(TTN)
|
XP_024308867.1:p.Glu16701Asp
|
|
XM_024453100.1:c.39957A>T
(TTN)
|
XP_024308868.1:p.Glu13319Asp
|
|