ENST00000342992.11:c.62337T>C
(TTN)
|
ENSP00000343764.6:p.Asp20779=
|
|
ENST00000342175.11:c.43422T>C
(TTN)
|
ENSP00000340554.6:p.Asp14474=
|
|
ENST00000359218.10:c.43221T>C
(TTN)
|
ENSP00000352154.5:p.Asp14407=
|
|
ENST00000342175.10:c.43422T>C
(TTN)
|
ENSP00000340554.6:p.Asp14474=
|
|
ENST00000342992.10:c.62337T>C
(TTN)
|
ENSP00000343764.6:p.Asp20779=
|
|
ENST00000359218.9:c.43221T>C
(TTN)
|
ENSP00000352154.5:p.Asp14407=
|
|
ENST00000460472.6:c.42846T>C
(TTN)
|
ENSP00000434586.1:p.Asp14282=
|
|
ENST00000589042.5:c.70041T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp23347=
|
|
ENST00000591111.5:c.65118T>C
(TTN)
|
ENSP00000465570.1:p.Asp21706=
|
|
ENST00000615779.4:c.65118T>C
(TTN)
|
ENSP00000483597.1:p.Asp21706=
|
|
NM_001256850.1:c.65118T>C
(TTN)
|
NP_001243779.1:p.Asp21706=
|
|
NM_001267550.2:c.70041T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp23347=
|
|
NM_003319.4:c.42846T>C
(TTN)
|
NP_003310.4:p.Asp14282=
|
|
NM_133378.4:c.62337T>C
(TTN)
|
NP_596869.4:p.Asp20779=
|
|
NM_133432.3:c.43221T>C
(TTN)
|
NP_597676.3:p.Asp14407=
|
|
NM_133437.4:c.43422T>C
(TTN)
|
NP_597681.4:p.Asp14474=
|
|
NR_038271.1:n.596+4642A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-6481A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.69138T>C
(TTN)
|
XP_011510031.1:p.Asp23046=
|
|
XM_011511730.1:c.43032T>C
(TTN)
|
XP_011510032.1:p.Asp14344=
|
|
XM_011511731.1:c.42891T>C
(TTN)
|
XP_011510033.1:p.Asp14297=
|
|
XM_017004819.1:c.68934T>C
(TTN)
|
XP_016860308.1:p.Asp22978=
|
|
XM_017004820.1:c.64332T>C
(TTN)
|
XP_016860309.1:p.Asp21444=
|
|
XM_017004821.1:c.64329T>C
(TTN)
|
XP_016860310.1:p.Asp21443=
|
|
XM_017004822.1:c.61371T>C
(TTN)
|
XP_016860311.1:p.Asp20457=
|
|
XM_017004823.1:c.42987T>C
(TTN)
|
XP_016860312.1:p.Asp14329=
|
|
XM_024453094.1:c.64482T>C
(TTN)
|
XP_024308862.1:p.Asp21494=
|
|
XM_024453095.1:c.64479T>C
(TTN)
|
XP_024308863.1:p.Asp21493=
|
|
XM_024453096.1:c.63912T>C
(TTN)
|
XP_024308864.1:p.Asp21304=
|
|
XM_024453097.1:c.61254T>C
(TTN)
|
XP_024308865.1:p.Asp20418=
|
|
XM_024453098.1:c.61173T>C
(TTN)
|
XP_024308866.1:p.Asp20391=
|
|
XM_024453099.1:c.42936T>C
(TTN)
|
XP_024308867.1:p.Asp14312=
|
|
XM_024453100.1:c.32790T>C
(TTN)
|
XP_024308868.1:p.Asp10930=
|
|