ENST00000342992.11:c.63634A>T
(TTN)
|
ENSP00000343764.6:p.Thr21212Ser
|
|
ENST00000342175.11:c.44719A>T
(TTN)
|
ENSP00000340554.6:p.Thr14907Ser
|
|
ENST00000359218.10:c.44518A>T
(TTN)
|
ENSP00000352154.5:p.Thr14840Ser
|
|
ENST00000342175.10:c.44719A>T
(TTN)
|
ENSP00000340554.6:p.Thr14907Ser
|
|
ENST00000342992.10:c.63634A>T
(TTN)
|
ENSP00000343764.6:p.Thr21212Ser
|
|
ENST00000359218.9:c.44518A>T
(TTN)
|
ENSP00000352154.5:p.Thr14840Ser
|
|
ENST00000460472.6:c.44143A>T
(TTN)
|
ENSP00000434586.1:p.Thr14715Ser
|
|
ENST00000589042.5:c.71338A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr23780Ser
|
|
ENST00000591111.5:c.66415A>T
(TTN)
|
ENSP00000465570.1:p.Thr22139Ser
|
|
ENST00000615779.4:c.66415A>T
(TTN)
|
ENSP00000483597.1:p.Thr22139Ser
|
|
NM_001256850.1:c.66415A>T
(TTN)
|
NP_001243779.1:p.Thr22139Ser
|
|
NM_001267550.2:c.71338A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Thr23780Ser
|
|
NM_003319.4:c.44143A>T
(TTN)
|
NP_003310.4:p.Thr14715Ser
|
|
NM_133378.4:c.63634A>T
(TTN)
|
NP_596869.4:p.Thr21212Ser
|
|
NM_133432.3:c.44518A>T
(TTN)
|
NP_597676.3:p.Thr14840Ser
|
|
NM_133437.4:c.44719A>T
(TTN)
|
NP_597681.4:p.Thr14907Ser
|
|
NR_038271.1:n.596+3345T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-7778T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.70435A>T
(TTN)
|
XP_011510031.1:p.Thr23479Ser
|
|
XM_011511730.1:c.44329A>T
(TTN)
|
XP_011510032.1:p.Thr14777Ser
|
|
XM_011511731.1:c.44188A>T
(TTN)
|
XP_011510033.1:p.Thr14730Ser
|
|
XM_017004819.1:c.70231A>T
(TTN)
|
XP_016860308.1:p.Thr23411Ser
|
|
XM_017004820.1:c.65629A>T
(TTN)
|
XP_016860309.1:p.Thr21877Ser
|
|
XM_017004821.1:c.65626A>T
(TTN)
|
XP_016860310.1:p.Thr21876Ser
|
|
XM_017004822.1:c.62668A>T
(TTN)
|
XP_016860311.1:p.Thr20890Ser
|
|
XM_017004823.1:c.44284A>T
(TTN)
|
XP_016860312.1:p.Thr14762Ser
|
|
XM_024453094.1:c.65779A>T
(TTN)
|
XP_024308862.1:p.Thr21927Ser
|
|
XM_024453095.1:c.65776A>T
(TTN)
|
XP_024308863.1:p.Thr21926Ser
|
|
XM_024453096.1:c.65209A>T
(TTN)
|
XP_024308864.1:p.Thr21737Ser
|
|
XM_024453097.1:c.62551A>T
(TTN)
|
XP_024308865.1:p.Thr20851Ser
|
|
XM_024453098.1:c.62470A>T
(TTN)
|
XP_024308866.1:p.Thr20824Ser
|
|
XM_024453099.1:c.44233A>T
(TTN)
|
XP_024308867.1:p.Thr14745Ser
|
|
XM_024453100.1:c.34087A>T
(TTN)
|
XP_024308868.1:p.Thr11363Ser
|
|