ENST00000342992.11:c.88201G>C
(TTN)
|
ENSP00000343764.6:p.Glu29401Gln
|
|
ENST00000342175.11:c.69286G>C
(TTN)
|
ENSP00000340554.6:p.Glu23096Gln
|
|
ENST00000359218.10:c.69085G>C
(TTN)
|
ENSP00000352154.5:p.Glu23029Gln
|
|
ENST00000342175.10:c.69286G>C
(TTN)
|
ENSP00000340554.6:p.Glu23096Gln
|
|
ENST00000342992.10:c.88201G>C
(TTN)
|
ENSP00000343764.6:p.Glu29401Gln
|
|
ENST00000359218.9:c.69085G>C
(TTN)
|
ENSP00000352154.5:p.Glu23029Gln
|
|
ENST00000460472.6:c.68710G>C
(TTN)
|
ENSP00000434586.1:p.Glu22904Gln
|
|
ENST00000589042.5:c.95905G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu31969Gln
|
|
ENST00000591111.5:c.90982G>C
(TTN)
|
ENSP00000465570.1:p.Glu30328Gln
|
|
ENST00000615779.4:c.90982G>C
(TTN)
|
ENSP00000483597.1:p.Glu30328Gln
|
|
NM_001256850.1:c.90982G>C
(TTN)
|
NP_001243779.1:p.Glu30328Gln
|
|
NM_001267550.2:c.95905G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu31969Gln
|
|
NM_003319.4:c.68710G>C
(TTN)
|
NP_003310.4:p.Glu22904Gln
|
|
NM_133378.4:c.88201G>C
(TTN)
|
NP_596869.4:p.Glu29401Gln
|
|
NM_133432.3:c.69085G>C
(TTN)
|
NP_597676.3:p.Glu23029Gln
|
|
NM_133437.4:c.69286G>C
(TTN)
|
NP_597681.4:p.Glu23096Gln
|
|
NR_038271.1:n.446+20688C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1963C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.95002G>C
(TTN)
|
XP_011510031.1:p.Glu31668Gln
|
|
XM_011511730.1:c.68896G>C
(TTN)
|
XP_011510032.1:p.Glu22966Gln
|
|
XM_011511731.1:c.68755G>C
(TTN)
|
XP_011510033.1:p.Glu22919Gln
|
|
XM_017004819.1:c.94798G>C
(TTN)
|
XP_016860308.1:p.Glu31600Gln
|
|
XM_017004820.1:c.90196G>C
(TTN)
|
XP_016860309.1:p.Glu30066Gln
|
|
XM_017004821.1:c.90193G>C
(TTN)
|
XP_016860310.1:p.Glu30065Gln
|
|
XM_017004822.1:c.87235G>C
(TTN)
|
XP_016860311.1:p.Glu29079Gln
|
|
XM_017004823.1:c.68851G>C
(TTN)
|
XP_016860312.1:p.Glu22951Gln
|
|
XM_024453094.1:c.90346G>C
(TTN)
|
XP_024308862.1:p.Glu30116Gln
|
|
XM_024453095.1:c.90343G>C
(TTN)
|
XP_024308863.1:p.Glu30115Gln
|
|
XM_024453096.1:c.89776G>C
(TTN)
|
XP_024308864.1:p.Glu29926Gln
|
|
XM_024453097.1:c.87118G>C
(TTN)
|
XP_024308865.1:p.Glu29040Gln
|
|
XM_024453098.1:c.87037G>C
(TTN)
|
XP_024308866.1:p.Glu29013Gln
|
|
XM_024453099.1:c.68800G>C
(TTN)
|
XP_024308867.1:p.Glu22934Gln
|
|
XM_024453100.1:c.58654G>C
(TTN)
|
XP_024308868.1:p.Glu19552Gln
|
|