ENST00000342992.11:c.69692A>T
(TTN)
|
ENSP00000343764.6:p.Asp23231Val
|
|
ENST00000342175.11:c.50777A>T
(TTN)
|
ENSP00000340554.6:p.Asp16926Val
|
|
ENST00000359218.10:c.50576A>T
(TTN)
|
ENSP00000352154.5:p.Asp16859Val
|
|
ENST00000342175.10:c.50777A>T
(TTN)
|
ENSP00000340554.6:p.Asp16926Val
|
|
ENST00000342992.10:c.69692A>T
(TTN)
|
ENSP00000343764.6:p.Asp23231Val
|
|
ENST00000359218.9:c.50576A>T
(TTN)
|
ENSP00000352154.5:p.Asp16859Val
|
|
ENST00000460472.6:c.50201A>T
(TTN)
|
ENSP00000434586.1:p.Asp16734Val
|
|
ENST00000589042.5:c.77396A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp25799Val
|
|
ENST00000591111.5:c.72473A>T
(TTN)
|
ENSP00000465570.1:p.Asp24158Val
|
|
ENST00000615779.4:c.72473A>T
(TTN)
|
ENSP00000483597.1:p.Asp24158Val
|
|
NM_001256850.1:c.72473A>T
(TTN)
|
NP_001243779.1:p.Asp24158Val
|
|
NM_001267550.2:c.77396A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp25799Val
|
|
NM_003319.4:c.50201A>T
(TTN)
|
NP_003310.4:p.Asp16734Val
|
|
NM_133378.4:c.69692A>T
(TTN)
|
NP_596869.4:p.Asp23231Val
|
|
NM_133432.3:c.50576A>T
(TTN)
|
NP_597676.3:p.Asp16859Val
|
|
NM_133437.4:c.50777A>T
(TTN)
|
NP_597681.4:p.Asp16926Val
|
|
NR_038271.1:n.447-2564T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13836T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.76493A>T
(TTN)
|
XP_011510031.1:p.Asp25498Val
|
|
XM_011511730.1:c.50387A>T
(TTN)
|
XP_011510032.1:p.Asp16796Val
|
|
XM_011511731.1:c.50246A>T
(TTN)
|
XP_011510033.1:p.Asp16749Val
|
|
XM_017004819.1:c.76289A>T
(TTN)
|
XP_016860308.1:p.Asp25430Val
|
|
XM_017004820.1:c.71687A>T
(TTN)
|
XP_016860309.1:p.Asp23896Val
|
|
XM_017004821.1:c.71684A>T
(TTN)
|
XP_016860310.1:p.Asp23895Val
|
|
XM_017004822.1:c.68726A>T
(TTN)
|
XP_016860311.1:p.Asp22909Val
|
|
XM_017004823.1:c.50342A>T
(TTN)
|
XP_016860312.1:p.Asp16781Val
|
|
XM_024453094.1:c.71837A>T
(TTN)
|
XP_024308862.1:p.Asp23946Val
|
|
XM_024453095.1:c.71834A>T
(TTN)
|
XP_024308863.1:p.Asp23945Val
|
|
XM_024453096.1:c.71267A>T
(TTN)
|
XP_024308864.1:p.Asp23756Val
|
|
XM_024453097.1:c.68609A>T
(TTN)
|
XP_024308865.1:p.Asp22870Val
|
|
XM_024453098.1:c.68528A>T
(TTN)
|
XP_024308866.1:p.Asp22843Val
|
|
XM_024453099.1:c.50291A>T
(TTN)
|
XP_024308867.1:p.Asp16764Val
|
|
XM_024453100.1:c.40145A>T
(TTN)
|
XP_024308868.1:p.Asp13382Val
|
|