ENST00000342992.11:c.92242G>T
(TTN)
|
ENSP00000343764.6:p.Ala30748Ser
|
|
ENST00000342175.11:c.73327G>T
(TTN)
|
ENSP00000340554.6:p.Ala24443Ser
|
|
ENST00000359218.10:c.73126G>T
(TTN)
|
ENSP00000352154.5:p.Ala24376Ser
|
|
ENST00000342175.10:c.73327G>T
(TTN)
|
ENSP00000340554.6:p.Ala24443Ser
|
|
ENST00000342992.10:c.92242G>T
(TTN)
|
ENSP00000343764.6:p.Ala30748Ser
|
|
ENST00000359218.9:c.73126G>T
(TTN)
|
ENSP00000352154.5:p.Ala24376Ser
|
|
ENST00000460472.6:c.72751G>T
(TTN)
|
ENSP00000434586.1:p.Ala24251Ser
|
|
ENST00000589042.5:c.99946G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala33316Ser
|
|
ENST00000591111.5:c.95023G>T
(TTN)
|
ENSP00000465570.1:p.Ala31675Ser
|
|
ENST00000615779.4:c.95023G>T
(TTN)
|
ENSP00000483597.1:p.Ala31675Ser
|
|
NM_001256850.1:c.95023G>T
(TTN)
|
NP_001243779.1:p.Ala31675Ser
|
|
NM_001267550.2:c.99946G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala33316Ser
|
|
NM_003319.4:c.72751G>T
(TTN)
|
NP_003310.4:p.Ala24251Ser
|
|
NM_133378.4:c.92242G>T
(TTN)
|
NP_596869.4:p.Ala30748Ser
|
|
NM_133432.3:c.73126G>T
(TTN)
|
NP_597676.3:p.Ala24376Ser
|
|
NM_133437.4:c.73327G>T
(TTN)
|
NP_597681.4:p.Ala24443Ser
|
|
NR_038271.1:n.446+13527C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.317-198C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.99043G>T
(TTN)
|
XP_011510031.1:p.Ala33015Ser
|
|
XM_011511730.1:c.72937G>T
(TTN)
|
XP_011510032.1:p.Ala24313Ser
|
|
XM_011511731.1:c.72796G>T
(TTN)
|
XP_011510033.1:p.Ala24266Ser
|
|
XM_017004819.1:c.98839G>T
(TTN)
|
XP_016860308.1:p.Ala32947Ser
|
|
XM_017004820.1:c.94237G>T
(TTN)
|
XP_016860309.1:p.Ala31413Ser
|
|
XM_017004821.1:c.94234G>T
(TTN)
|
XP_016860310.1:p.Ala31412Ser
|
|
XM_017004822.1:c.91276G>T
(TTN)
|
XP_016860311.1:p.Ala30426Ser
|
|
XM_017004823.1:c.72892G>T
(TTN)
|
XP_016860312.1:p.Ala24298Ser
|
|
XM_024453094.1:c.94387G>T
(TTN)
|
XP_024308862.1:p.Ala31463Ser
|
|
XM_024453095.1:c.94384G>T
(TTN)
|
XP_024308863.1:p.Ala31462Ser
|
|
XM_024453096.1:c.93817G>T
(TTN)
|
XP_024308864.1:p.Ala31273Ser
|
|
XM_024453097.1:c.91159G>T
(TTN)
|
XP_024308865.1:p.Ala30387Ser
|
|
XM_024453098.1:c.91078G>T
(TTN)
|
XP_024308866.1:p.Ala30360Ser
|
|
XM_024453099.1:c.72841G>T
(TTN)
|
XP_024308867.1:p.Ala24281Ser
|
|
XM_024453100.1:c.62695G>T
(TTN)
|
XP_024308868.1:p.Ala20899Ser
|
|