|
NM_001267550.2:c.52449C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Thr17483=
|
|
ENST00000589042.5:c.52449C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr17483=
|
|
NM_001256850.1:c.47526C>T
(TTN)
|
NP_001243779.1:p.Thr15842=
|
|
NM_003319.4:c.25254C>T
(TTN)
|
NP_003310.4:p.Thr8418=
|
|
NM_133378.4:c.44745C>T
(TTN)
|
NP_596869.4:p.Thr14915=
|
|
NM_133432.3:c.25629C>T
(TTN)
|
NP_597676.3:p.Thr8543=
|
|
NM_133437.4:c.25830C>T
(TTN)
|
NP_597681.4:p.Thr8610=
|
|
NR_038271.1:n.782+168G>A
(TTN-AS1)
|
|
|
ENST00000342175.10:c.25830C>T
(TTN)
|
ENSP00000340554.6:p.Thr8610=
|
|
ENST00000342175.11:c.25830C>T
(TTN)
|
ENSP00000340554.6:p.Thr8610=
|
|
ENST00000342992.10:c.44745C>T
(TTN)
|
ENSP00000343764.6:p.Thr14915=
|
|
ENST00000342992.11:c.44745C>T
(TTN)
|
ENSP00000343764.6:p.Thr14915=
|
|
ENST00000359218.10:c.25629C>T
(TTN)
|
ENSP00000352154.5:p.Thr8543=
|
|
ENST00000359218.9:c.25629C>T
(TTN)
|
ENSP00000352154.5:p.Thr8543=
|
|
ENST00000460472.6:c.25254C>T
(TTN)
|
ENSP00000434586.1:p.Thr8418=
|
|
ENST00000591111.5:c.47526C>T
(TTN)
|
ENSP00000465570.1:p.Thr15842=
|
|
ENST00000615779.4:c.47526C>T
(TTN)
|
ENSP00000483597.1:p.Thr15842=
|
|
XM_011511729.1:c.51546C>T
(TTN)
|
XP_011510031.1:p.Thr17182=
|
|
XM_011511730.1:c.25440C>T
(TTN)
|
XP_011510032.1:p.Thr8480=
|
|
XM_011511731.1:c.25299C>T
(TTN)
|
XP_011510033.1:p.Thr8433=
|
|
XM_017004819.1:c.51342C>T
(TTN)
|
XP_016860308.1:p.Thr17114=
|
|
XM_017004820.1:c.46740C>T
(TTN)
|
XP_016860309.1:p.Thr15580=
|
|
XM_017004821.1:c.46737C>T
(TTN)
|
XP_016860310.1:p.Thr15579=
|
|
XM_017004822.1:c.43779C>T
(TTN)
|
XP_016860311.1:p.Thr14593=
|
|
XM_017004823.1:c.25395C>T
(TTN)
|
XP_016860312.1:p.Thr8465=
|
|
XM_024453094.1:c.46890C>T
(TTN)
|
XP_024308862.1:p.Thr15630=
|
|
XM_024453095.1:c.46887C>T
(TTN)
|
XP_024308863.1:p.Thr15629=
|
|
XM_024453096.1:c.46320C>T
(TTN)
|
XP_024308864.1:p.Thr15440=
|
|
XM_024453097.1:c.43662C>T
(TTN)
|
XP_024308865.1:p.Thr14554=
|
|
XM_024453098.1:c.43581C>T
(TTN)
|
XP_024308866.1:p.Thr14527=
|
|
XM_024453099.1:c.25344C>T
(TTN)
|
XP_024308867.1:p.Thr8448=
|
|
XM_024453100.1:c.15198C>T
(TTN)
|
XP_024308868.1:p.Thr5066=
|
