|
ENST00000342992.11:c.95670C>T
(TTN)
|
ENSP00000343764.6:p.Tyr31890=
|
|
|
ENST00000342175.11:c.76755C>T
(TTN)
|
ENSP00000340554.6:p.Tyr25585=
|
|
|
ENST00000359218.10:c.76554C>T
(TTN)
|
ENSP00000352154.5:p.Tyr25518=
|
|
|
ENST00000342175.10:c.76755C>T
(TTN)
|
ENSP00000340554.6:p.Tyr25585=
|
|
|
ENST00000342992.10:c.95670C>T
(TTN)
|
ENSP00000343764.6:p.Tyr31890=
|
|
|
ENST00000359218.9:c.76554C>T
(TTN)
|
ENSP00000352154.5:p.Tyr25518=
|
|
|
ENST00000460472.6:c.76179C>T
(TTN)
|
ENSP00000434586.1:p.Tyr25393=
|
|
|
ENST00000589042.5:c.103374C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr34458=
|
|
|
ENST00000591111.5:c.98451C>T
(TTN)
|
ENSP00000465570.1:p.Tyr32817=
|
|
|
ENST00000615779.4:c.98451C>T
(TTN)
|
ENSP00000483597.1:p.Tyr32817=
|
|
|
NM_001256850.1:c.98451C>T
(TTN)
|
NP_001243779.1:p.Tyr32817=
|
|
|
NM_001267550.2:c.103374C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr34458=
|
|
|
NM_003319.4:c.76179C>T
(TTN)
|
NP_003310.4:p.Tyr25393=
|
|
|
NM_133378.4:c.95670C>T
(TTN)
|
NP_596869.4:p.Tyr31890=
|
|
|
NM_133432.3:c.76554C>T
(TTN)
|
NP_597676.3:p.Tyr25518=
|
|
|
NM_133437.4:c.76755C>T
(TTN)
|
NP_597681.4:p.Tyr25585=
|
|
|
NR_038271.1:n.446+9605G>A
(TTN-AS1)
|
|
|
|
NR_038272.1:n.220-2491G>A
(TTN-AS1)
|
|
|
|
XM_011511729.1:c.102471C>T
(TTN)
|
XP_011510031.1:p.Tyr34157=
|
|
|
XM_011511730.1:c.76365C>T
(TTN)
|
XP_011510032.1:p.Tyr25455=
|
|
|
XM_011511731.1:c.76224C>T
(TTN)
|
XP_011510033.1:p.Tyr25408=
|
|
|
XM_017004819.1:c.102267C>T
(TTN)
|
XP_016860308.1:p.Tyr34089=
|
|
|
XM_017004820.1:c.97665C>T
(TTN)
|
XP_016860309.1:p.Tyr32555=
|
|
|
XM_017004821.1:c.97662C>T
(TTN)
|
XP_016860310.1:p.Tyr32554=
|
|
|
XM_017004822.1:c.94704C>T
(TTN)
|
XP_016860311.1:p.Tyr31568=
|
|
|
XM_017004823.1:c.76320C>T
(TTN)
|
XP_016860312.1:p.Tyr25440=
|
|
|
XM_024453094.1:c.97815C>T
(TTN)
|
XP_024308862.1:p.Tyr32605=
|
|
|
XM_024453095.1:c.97812C>T
(TTN)
|
XP_024308863.1:p.Tyr32604=
|
|
|
XM_024453096.1:c.97245C>T
(TTN)
|
XP_024308864.1:p.Tyr32415=
|
|
|
XM_024453097.1:c.94587C>T
(TTN)
|
XP_024308865.1:p.Tyr31529=
|
|
|
XM_024453098.1:c.94506C>T
(TTN)
|
XP_024308866.1:p.Tyr31502=
|
|
|
XM_024453099.1:c.76269C>T
(TTN)
|
XP_024308867.1:p.Tyr25423=
|
|
|
XM_024453100.1:c.66123C>T
(TTN)
|
XP_024308868.1:p.Tyr22041=
|
|
