ENST00000342992.11:c.96636C>A
(TTN)
|
ENSP00000343764.6:p.Thr32212=
|
|
ENST00000342175.11:c.77721C>A
(TTN)
|
ENSP00000340554.6:p.Thr25907=
|
|
ENST00000359218.10:c.77520C>A
(TTN)
|
ENSP00000352154.5:p.Thr25840=
|
|
ENST00000342175.10:c.77721C>A
(TTN)
|
ENSP00000340554.6:p.Thr25907=
|
|
ENST00000342992.10:c.96636C>A
(TTN)
|
ENSP00000343764.6:p.Thr32212=
|
|
ENST00000359218.9:c.77520C>A
(TTN)
|
ENSP00000352154.5:p.Thr25840=
|
|
ENST00000460472.6:c.77145C>A
(TTN)
|
ENSP00000434586.1:p.Thr25715=
|
|
ENST00000589042.5:c.104340C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr34780=
|
|
ENST00000591111.5:c.99417C>A
(TTN)
|
ENSP00000465570.1:p.Thr33139=
|
|
ENST00000615779.4:c.99417C>A
(TTN)
|
ENSP00000483597.1:p.Thr33139=
|
|
NM_001256850.1:c.99417C>A
(TTN)
|
NP_001243779.1:p.Thr33139=
|
|
NM_001267550.2:c.104340C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr34780=
|
|
NM_003319.4:c.77145C>A
(TTN)
|
NP_003310.4:p.Thr25715=
|
|
NM_133378.4:c.96636C>A
(TTN)
|
NP_596869.4:p.Thr32212=
|
|
NM_133432.3:c.77520C>A
(TTN)
|
NP_597676.3:p.Thr25840=
|
|
NM_133437.4:c.77721C>A
(TTN)
|
NP_597681.4:p.Thr25907=
|
|
NR_038271.1:n.446+8639G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3457G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103437C>A
(TTN)
|
XP_011510031.1:p.Thr34479=
|
|
XM_011511730.1:c.77331C>A
(TTN)
|
XP_011510032.1:p.Thr25777=
|
|
XM_011511731.1:c.77190C>A
(TTN)
|
XP_011510033.1:p.Thr25730=
|
|
XM_017004819.1:c.103233C>A
(TTN)
|
XP_016860308.1:p.Thr34411=
|
|
XM_017004820.1:c.98631C>A
(TTN)
|
XP_016860309.1:p.Thr32877=
|
|
XM_017004821.1:c.98628C>A
(TTN)
|
XP_016860310.1:p.Thr32876=
|
|
XM_017004822.1:c.95670C>A
(TTN)
|
XP_016860311.1:p.Thr31890=
|
|
XM_017004823.1:c.77286C>A
(TTN)
|
XP_016860312.1:p.Thr25762=
|
|
XM_024453094.1:c.98781C>A
(TTN)
|
XP_024308862.1:p.Thr32927=
|
|
XM_024453095.1:c.98778C>A
(TTN)
|
XP_024308863.1:p.Thr32926=
|
|
XM_024453096.1:c.98211C>A
(TTN)
|
XP_024308864.1:p.Thr32737=
|
|
XM_024453097.1:c.95553C>A
(TTN)
|
XP_024308865.1:p.Thr31851=
|
|
XM_024453098.1:c.95472C>A
(TTN)
|
XP_024308866.1:p.Thr31824=
|
|
XM_024453099.1:c.77235C>A
(TTN)
|
XP_024308867.1:p.Thr25745=
|
|
XM_024453100.1:c.67089C>A
(TTN)
|
XP_024308868.1:p.Thr22363=
|
|