ENST00000342992.11:c.83337T>A
(TTN)
|
ENSP00000343764.6:p.Ala27779=
|
|
ENST00000342175.11:c.64422T>A
(TTN)
|
ENSP00000340554.6:p.Ala21474=
|
|
ENST00000359218.10:c.64221T>A
(TTN)
|
ENSP00000352154.5:p.Ala21407=
|
|
ENST00000342175.10:c.64422T>A
(TTN)
|
ENSP00000340554.6:p.Ala21474=
|
|
ENST00000342992.10:c.83337T>A
(TTN)
|
ENSP00000343764.6:p.Ala27779=
|
|
ENST00000359218.9:c.64221T>A
(TTN)
|
ENSP00000352154.5:p.Ala21407=
|
|
ENST00000460472.6:c.63846T>A
(TTN)
|
ENSP00000434586.1:p.Ala21282=
|
|
ENST00000589042.5:c.91041T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala30347=
|
|
ENST00000591111.5:c.86118T>A
(TTN)
|
ENSP00000465570.1:p.Ala28706=
|
|
ENST00000615779.4:c.86118T>A
(TTN)
|
ENSP00000483597.1:p.Ala28706=
|
|
NM_001256850.1:c.86118T>A
(TTN)
|
NP_001243779.1:p.Ala28706=
|
|
NM_001267550.2:c.91041T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala30347=
|
|
NM_003319.4:c.63846T>A
(TTN)
|
NP_003310.4:p.Ala21282=
|
|
NM_133378.4:c.83337T>A
(TTN)
|
NP_596869.4:p.Ala27779=
|
|
NM_133432.3:c.64221T>A
(TTN)
|
NP_597676.3:p.Ala21407=
|
|
NM_133437.4:c.64422T>A
(TTN)
|
NP_597681.4:p.Ala21474=
|
|
NR_038271.1:n.447-19441A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9498A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.90138T>A
(TTN)
|
XP_011510031.1:p.Ala30046=
|
|
XM_011511730.1:c.64032T>A
(TTN)
|
XP_011510032.1:p.Ala21344=
|
|
XM_011511731.1:c.63891T>A
(TTN)
|
XP_011510033.1:p.Ala21297=
|
|
XM_017004819.1:c.89934T>A
(TTN)
|
XP_016860308.1:p.Ala29978=
|
|
XM_017004820.1:c.85332T>A
(TTN)
|
XP_016860309.1:p.Ala28444=
|
|
XM_017004821.1:c.85329T>A
(TTN)
|
XP_016860310.1:p.Ala28443=
|
|
XM_017004822.1:c.82371T>A
(TTN)
|
XP_016860311.1:p.Ala27457=
|
|
XM_017004823.1:c.63987T>A
(TTN)
|
XP_016860312.1:p.Ala21329=
|
|
XM_024453094.1:c.85482T>A
(TTN)
|
XP_024308862.1:p.Ala28494=
|
|
XM_024453095.1:c.85479T>A
(TTN)
|
XP_024308863.1:p.Ala28493=
|
|
XM_024453096.1:c.84912T>A
(TTN)
|
XP_024308864.1:p.Ala28304=
|
|
XM_024453097.1:c.82254T>A
(TTN)
|
XP_024308865.1:p.Ala27418=
|
|
XM_024453098.1:c.82173T>A
(TTN)
|
XP_024308866.1:p.Ala27391=
|
|
XM_024453099.1:c.63936T>A
(TTN)
|
XP_024308867.1:p.Ala21312=
|
|
XM_024453100.1:c.53790T>A
(TTN)
|
XP_024308868.1:p.Ala17930=
|
|