ENST00000342992.11:c.92340G>A
(TTN)
|
ENSP00000343764.6:p.Val30780=
|
|
ENST00000342175.11:c.73425G>A
(TTN)
|
ENSP00000340554.6:p.Val24475=
|
|
ENST00000359218.10:c.73224G>A
(TTN)
|
ENSP00000352154.5:p.Val24408=
|
|
ENST00000342175.10:c.73425G>A
(TTN)
|
ENSP00000340554.6:p.Val24475=
|
|
ENST00000342992.10:c.92340G>A
(TTN)
|
ENSP00000343764.6:p.Val30780=
|
|
ENST00000359218.9:c.73224G>A
(TTN)
|
ENSP00000352154.5:p.Val24408=
|
|
ENST00000460472.6:c.72849G>A
(TTN)
|
ENSP00000434586.1:p.Val24283=
|
|
ENST00000589042.5:c.100044G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val33348=
|
|
ENST00000591111.5:c.95121G>A
(TTN)
|
ENSP00000465570.1:p.Val31707=
|
|
ENST00000615779.4:c.95121G>A
(TTN)
|
ENSP00000483597.1:p.Val31707=
|
|
NM_001256850.1:c.95121G>A
(TTN)
|
NP_001243779.1:p.Val31707=
|
|
NM_001267550.2:c.100044G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Val33348=
|
|
NM_003319.4:c.72849G>A
(TTN)
|
NP_003310.4:p.Val24283=
|
|
NM_133378.4:c.92340G>A
(TTN)
|
NP_596869.4:p.Val30780=
|
|
NM_133432.3:c.73224G>A
(TTN)
|
NP_597676.3:p.Val24408=
|
|
NM_133437.4:c.73425G>A
(TTN)
|
NP_597681.4:p.Val24475=
|
|
NR_038271.1:n.446+13429C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.317-296C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.99141G>A
(TTN)
|
XP_011510031.1:p.Val33047=
|
|
XM_011511730.1:c.73035G>A
(TTN)
|
XP_011510032.1:p.Val24345=
|
|
XM_011511731.1:c.72894G>A
(TTN)
|
XP_011510033.1:p.Val24298=
|
|
XM_017004819.1:c.98937G>A
(TTN)
|
XP_016860308.1:p.Val32979=
|
|
XM_017004820.1:c.94335G>A
(TTN)
|
XP_016860309.1:p.Val31445=
|
|
XM_017004821.1:c.94332G>A
(TTN)
|
XP_016860310.1:p.Val31444=
|
|
XM_017004822.1:c.91374G>A
(TTN)
|
XP_016860311.1:p.Val30458=
|
|
XM_017004823.1:c.72990G>A
(TTN)
|
XP_016860312.1:p.Val24330=
|
|
XM_024453094.1:c.94485G>A
(TTN)
|
XP_024308862.1:p.Val31495=
|
|
XM_024453095.1:c.94482G>A
(TTN)
|
XP_024308863.1:p.Val31494=
|
|
XM_024453096.1:c.93915G>A
(TTN)
|
XP_024308864.1:p.Val31305=
|
|
XM_024453097.1:c.91257G>A
(TTN)
|
XP_024308865.1:p.Val30419=
|
|
XM_024453098.1:c.91176G>A
(TTN)
|
XP_024308866.1:p.Val30392=
|
|
XM_024453099.1:c.72939G>A
(TTN)
|
XP_024308867.1:p.Val24313=
|
|
XM_024453100.1:c.62793G>A
(TTN)
|
XP_024308868.1:p.Val20931=
|
|