ENST00000342992.11:c.98262T>A
(TTN)
|
ENSP00000343764.6:p.Asp32754Glu
|
|
ENST00000342175.11:c.79347T>A
(TTN)
|
ENSP00000340554.6:p.Asp26449Glu
|
|
ENST00000359218.10:c.79146T>A
(TTN)
|
ENSP00000352154.5:p.Asp26382Glu
|
|
ENST00000342175.10:c.79347T>A
(TTN)
|
ENSP00000340554.6:p.Asp26449Glu
|
|
ENST00000342992.10:c.98262T>A
(TTN)
|
ENSP00000343764.6:p.Asp32754Glu
|
|
ENST00000359218.9:c.79146T>A
(TTN)
|
ENSP00000352154.5:p.Asp26382Glu
|
|
ENST00000460472.6:c.78771T>A
(TTN)
|
ENSP00000434586.1:p.Asp26257Glu
|
|
ENST00000589042.5:c.105966T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp35322Glu
|
|
ENST00000591111.5:c.101043T>A
(TTN)
|
ENSP00000465570.1:p.Asp33681Glu
|
|
ENST00000615779.4:c.101043T>A
(TTN)
|
ENSP00000483597.1:p.Asp33681Glu
|
|
NM_001256850.1:c.101043T>A
(TTN)
|
NP_001243779.1:p.Asp33681Glu
|
|
NM_001267550.2:c.105966T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Asp35322Glu
|
|
NM_003319.4:c.78771T>A
(TTN)
|
NP_003310.4:p.Asp26257Glu
|
|
NM_133378.4:c.98262T>A
(TTN)
|
NP_596869.4:p.Asp32754Glu
|
|
NM_133432.3:c.79146T>A
(TTN)
|
NP_597676.3:p.Asp26382Glu
|
|
NM_133437.4:c.79347T>A
(TTN)
|
NP_597681.4:p.Asp26449Glu
|
|
NR_038271.1:n.446+7013A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5083A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105063T>A
(TTN)
|
XP_011510031.1:p.Asp35021Glu
|
|
XM_011511730.1:c.78957T>A
(TTN)
|
XP_011510032.1:p.Asp26319Glu
|
|
XM_011511731.1:c.78816T>A
(TTN)
|
XP_011510033.1:p.Asp26272Glu
|
|
XM_017004819.1:c.104859T>A
(TTN)
|
XP_016860308.1:p.Asp34953Glu
|
|
XM_017004820.1:c.100257T>A
(TTN)
|
XP_016860309.1:p.Asp33419Glu
|
|
XM_017004821.1:c.100254T>A
(TTN)
|
XP_016860310.1:p.Asp33418Glu
|
|
XM_017004822.1:c.97296T>A
(TTN)
|
XP_016860311.1:p.Asp32432Glu
|
|
XM_017004823.1:c.78912T>A
(TTN)
|
XP_016860312.1:p.Asp26304Glu
|
|
XM_024453094.1:c.100407T>A
(TTN)
|
XP_024308862.1:p.Asp33469Glu
|
|
XM_024453095.1:c.100404T>A
(TTN)
|
XP_024308863.1:p.Asp33468Glu
|
|
XM_024453096.1:c.99837T>A
(TTN)
|
XP_024308864.1:p.Asp33279Glu
|
|
XM_024453097.1:c.97179T>A
(TTN)
|
XP_024308865.1:p.Asp32393Glu
|
|
XM_024453098.1:c.97098T>A
(TTN)
|
XP_024308866.1:p.Asp32366Glu
|
|
XM_024453099.1:c.78861T>A
(TTN)
|
XP_024308867.1:p.Asp26287Glu
|
|
XM_024453100.1:c.68715T>A
(TTN)
|
XP_024308868.1:p.Asp22905Glu
|
|