ENST00000342992.11:c.64386G>A
(TTN)
|
ENSP00000343764.6:p.Lys21462=
|
|
ENST00000342175.11:c.45471G>A
(TTN)
|
ENSP00000340554.6:p.Lys15157=
|
|
ENST00000359218.10:c.45270G>A
(TTN)
|
ENSP00000352154.5:p.Lys15090=
|
|
ENST00000342175.10:c.45471G>A
(TTN)
|
ENSP00000340554.6:p.Lys15157=
|
|
ENST00000342992.10:c.64386G>A
(TTN)
|
ENSP00000343764.6:p.Lys21462=
|
|
ENST00000359218.9:c.45270G>A
(TTN)
|
ENSP00000352154.5:p.Lys15090=
|
|
ENST00000460472.6:c.44895G>A
(TTN)
|
ENSP00000434586.1:p.Lys14965=
|
|
ENST00000589042.5:c.72090G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys24030=
|
|
ENST00000591111.5:c.67167G>A
(TTN)
|
ENSP00000465570.1:p.Lys22389=
|
|
ENST00000615779.4:c.67167G>A
(TTN)
|
ENSP00000483597.1:p.Lys22389=
|
|
NM_001256850.1:c.67167G>A
(TTN)
|
NP_001243779.1:p.Lys22389=
|
|
NM_001267550.2:c.72090G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Lys24030=
|
|
NM_003319.4:c.44895G>A
(TTN)
|
NP_003310.4:p.Lys14965=
|
|
NM_133378.4:c.64386G>A
(TTN)
|
NP_596869.4:p.Lys21462=
|
|
NM_133432.3:c.45270G>A
(TTN)
|
NP_597676.3:p.Lys15090=
|
|
NM_133437.4:c.45471G>A
(TTN)
|
NP_597681.4:p.Lys15157=
|
|
NR_038271.1:n.596+2593C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-8530C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.71187G>A
(TTN)
|
XP_011510031.1:p.Lys23729=
|
|
XM_011511730.1:c.45081G>A
(TTN)
|
XP_011510032.1:p.Lys15027=
|
|
XM_011511731.1:c.44940G>A
(TTN)
|
XP_011510033.1:p.Lys14980=
|
|
XM_017004819.1:c.70983G>A
(TTN)
|
XP_016860308.1:p.Lys23661=
|
|
XM_017004820.1:c.66381G>A
(TTN)
|
XP_016860309.1:p.Lys22127=
|
|
XM_017004821.1:c.66378G>A
(TTN)
|
XP_016860310.1:p.Lys22126=
|
|
XM_017004822.1:c.63420G>A
(TTN)
|
XP_016860311.1:p.Lys21140=
|
|
XM_017004823.1:c.45036G>A
(TTN)
|
XP_016860312.1:p.Lys15012=
|
|
XM_024453094.1:c.66531G>A
(TTN)
|
XP_024308862.1:p.Lys22177=
|
|
XM_024453095.1:c.66528G>A
(TTN)
|
XP_024308863.1:p.Lys22176=
|
|
XM_024453096.1:c.65961G>A
(TTN)
|
XP_024308864.1:p.Lys21987=
|
|
XM_024453097.1:c.63303G>A
(TTN)
|
XP_024308865.1:p.Lys21101=
|
|
XM_024453098.1:c.63222G>A
(TTN)
|
XP_024308866.1:p.Lys21074=
|
|
XM_024453099.1:c.44985G>A
(TTN)
|
XP_024308867.1:p.Lys14995=
|
|
XM_024453100.1:c.34839G>A
(TTN)
|
XP_024308868.1:p.Lys11613=
|
|