|
NM_001267550.2:c.105360C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35120=
|
|
ENST00000589042.5:c.105360C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35120=
|
|
NM_001256850.1:c.100437C>T
(TTN)
|
NP_001243779.1:p.Thr33479=
|
|
NM_003319.4:c.78165C>T
(TTN)
|
NP_003310.4:p.Thr26055=
|
|
NM_133378.4:c.97656C>T
(TTN)
|
NP_596869.4:p.Thr32552=
|
|
NM_133432.3:c.78540C>T
(TTN)
|
NP_597676.3:p.Thr26180=
|
|
NM_133437.4:c.78741C>T
(TTN)
|
NP_597681.4:p.Thr26247=
|
|
NR_038271.1:n.446+7619G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-4477G>A
(TTN-AS1)
|
|
|
ENST00000342175.10:c.78741C>T
(TTN)
|
ENSP00000340554.6:p.Thr26247=
|
|
ENST00000342175.11:c.78741C>T
(TTN)
|
ENSP00000340554.6:p.Thr26247=
|
|
ENST00000342992.10:c.97656C>T
(TTN)
|
ENSP00000343764.6:p.Thr32552=
|
|
ENST00000342992.11:c.97656C>T
(TTN)
|
ENSP00000343764.6:p.Thr32552=
|
|
ENST00000359218.10:c.78540C>T
(TTN)
|
ENSP00000352154.5:p.Thr26180=
|
|
ENST00000359218.9:c.78540C>T
(TTN)
|
ENSP00000352154.5:p.Thr26180=
|
|
ENST00000460472.6:c.78165C>T
(TTN)
|
ENSP00000434586.1:p.Thr26055=
|
|
ENST00000591111.5:c.100437C>T
(TTN)
|
ENSP00000465570.1:p.Thr33479=
|
|
ENST00000615779.4:c.100437C>T
(TTN)
|
ENSP00000483597.1:p.Thr33479=
|
|
XM_011511729.1:c.104457C>T
(TTN)
|
XP_011510031.1:p.Thr34819=
|
|
XM_011511730.1:c.78351C>T
(TTN)
|
XP_011510032.1:p.Thr26117=
|
|
XM_011511731.1:c.78210C>T
(TTN)
|
XP_011510033.1:p.Thr26070=
|
|
XM_017004819.1:c.104253C>T
(TTN)
|
XP_016860308.1:p.Thr34751=
|
|
XM_017004820.1:c.99651C>T
(TTN)
|
XP_016860309.1:p.Thr33217=
|
|
XM_017004821.1:c.99648C>T
(TTN)
|
XP_016860310.1:p.Thr33216=
|
|
XM_017004822.1:c.96690C>T
(TTN)
|
XP_016860311.1:p.Thr32230=
|
|
XM_017004823.1:c.78306C>T
(TTN)
|
XP_016860312.1:p.Thr26102=
|
|
XM_024453094.1:c.99801C>T
(TTN)
|
XP_024308862.1:p.Thr33267=
|
|
XM_024453095.1:c.99798C>T
(TTN)
|
XP_024308863.1:p.Thr33266=
|
|
XM_024453096.1:c.99231C>T
(TTN)
|
XP_024308864.1:p.Thr33077=
|
|
XM_024453097.1:c.96573C>T
(TTN)
|
XP_024308865.1:p.Thr32191=
|
|
XM_024453098.1:c.96492C>T
(TTN)
|
XP_024308866.1:p.Thr32164=
|
|
XM_024453099.1:c.78255C>T
(TTN)
|
XP_024308867.1:p.Thr26085=
|
|
XM_024453100.1:c.68109C>T
(TTN)
|
XP_024308868.1:p.Thr22703=
|
