|
NM_001267550.2:c.75489C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Thr25163=
|
|
ENST00000589042.5:c.75489C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr25163=
|
|
NM_001256850.1:c.70566C>T
(TTN)
|
NP_001243779.1:p.Thr23522=
|
|
NM_003319.4:c.48294C>T
(TTN)
|
NP_003310.4:p.Thr16098=
|
|
NM_133378.4:c.67785C>T
(TTN)
|
NP_596869.4:p.Thr22595=
|
|
NM_133432.3:c.48669C>T
(TTN)
|
NP_597676.3:p.Thr16223=
|
|
NM_133437.4:c.48870C>T
(TTN)
|
NP_597681.4:p.Thr16290=
|
|
NR_038271.1:n.447-657G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-11929G>A
(TTN-AS1)
|
|
|
ENST00000342175.10:c.48870C>T
(TTN)
|
ENSP00000340554.6:p.Thr16290=
|
|
ENST00000342175.11:c.48870C>T
(TTN)
|
ENSP00000340554.6:p.Thr16290=
|
|
ENST00000342992.10:c.67785C>T
(TTN)
|
ENSP00000343764.6:p.Thr22595=
|
|
ENST00000342992.11:c.67785C>T
(TTN)
|
ENSP00000343764.6:p.Thr22595=
|
|
ENST00000359218.10:c.48669C>T
(TTN)
|
ENSP00000352154.5:p.Thr16223=
|
|
ENST00000359218.9:c.48669C>T
(TTN)
|
ENSP00000352154.5:p.Thr16223=
|
|
ENST00000460472.6:c.48294C>T
(TTN)
|
ENSP00000434586.1:p.Thr16098=
|
|
ENST00000591111.5:c.70566C>T
(TTN)
|
ENSP00000465570.1:p.Thr23522=
|
|
ENST00000615779.4:c.70566C>T
(TTN)
|
ENSP00000483597.1:p.Thr23522=
|
|
XM_011511729.1:c.74586C>T
(TTN)
|
XP_011510031.1:p.Thr24862=
|
|
XM_011511730.1:c.48480C>T
(TTN)
|
XP_011510032.1:p.Thr16160=
|
|
XM_011511731.1:c.48339C>T
(TTN)
|
XP_011510033.1:p.Thr16113=
|
|
XM_017004819.1:c.74382C>T
(TTN)
|
XP_016860308.1:p.Thr24794=
|
|
XM_017004820.1:c.69780C>T
(TTN)
|
XP_016860309.1:p.Thr23260=
|
|
XM_017004821.1:c.69777C>T
(TTN)
|
XP_016860310.1:p.Thr23259=
|
|
XM_017004822.1:c.66819C>T
(TTN)
|
XP_016860311.1:p.Thr22273=
|
|
XM_017004823.1:c.48435C>T
(TTN)
|
XP_016860312.1:p.Thr16145=
|
|
XM_024453094.1:c.69930C>T
(TTN)
|
XP_024308862.1:p.Thr23310=
|
|
XM_024453095.1:c.69927C>T
(TTN)
|
XP_024308863.1:p.Thr23309=
|
|
XM_024453096.1:c.69360C>T
(TTN)
|
XP_024308864.1:p.Thr23120=
|
|
XM_024453097.1:c.66702C>T
(TTN)
|
XP_024308865.1:p.Thr22234=
|
|
XM_024453098.1:c.66621C>T
(TTN)
|
XP_024308866.1:p.Thr22207=
|
|
XM_024453099.1:c.48384C>T
(TTN)
|
XP_024308867.1:p.Thr16128=
|
|
XM_024453100.1:c.38238C>T
(TTN)
|
XP_024308868.1:p.Thr12746=
|
