|
ENST00000342992.11:c.71899C>T
(TTN)
|
ENSP00000343764.6:p.Gln23967Ter
|
|
|
ENST00000342175.11:c.52984C>T
(TTN)
|
ENSP00000340554.6:p.Gln17662Ter
|
|
|
ENST00000359218.10:c.52783C>T
(TTN)
|
ENSP00000352154.5:p.Gln17595Ter
|
|
|
ENST00000342175.10:c.52984C>T
(TTN)
|
ENSP00000340554.6:p.Gln17662Ter
|
|
|
ENST00000342992.10:c.71899C>T
(TTN)
|
ENSP00000343764.6:p.Gln23967Ter
|
|
|
ENST00000359218.9:c.52783C>T
(TTN)
|
ENSP00000352154.5:p.Gln17595Ter
|
|
|
ENST00000460472.6:c.52408C>T
(TTN)
|
ENSP00000434586.1:p.Gln17470Ter
|
|
|
ENST00000589042.5:c.79603C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln26535Ter
|
|
|
ENST00000591111.5:c.74680C>T
(TTN)
|
ENSP00000465570.1:p.Gln24894Ter
|
|
|
ENST00000615779.4:c.74680C>T
(TTN)
|
ENSP00000483597.1:p.Gln24894Ter
|
|
|
NM_001256850.1:c.74680C>T
(TTN)
|
NP_001243779.1:p.Gln24894Ter
|
|
|
NM_001267550.2:c.79603C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gln26535Ter
|
|
|
NM_003319.4:c.52408C>T
(TTN)
|
NP_003310.4:p.Gln17470Ter
|
|
|
NM_133378.4:c.71899C>T
(TTN)
|
NP_596869.4:p.Gln23967Ter
|
|
|
NM_133432.3:c.52783C>T
(TTN)
|
NP_597676.3:p.Gln17595Ter
|
|
|
NM_133437.4:c.52984C>T
(TTN)
|
NP_597681.4:p.Gln17662Ter
|
|
|
NR_038271.1:n.447-4771G>A
(TTN-AS1)
|
|
|
|
NR_038272.1:n.2044-16043G>A
(TTN-AS1)
|
|
|
|
XM_011511729.1:c.78700C>T
(TTN)
|
XP_011510031.1:p.Gln26234Ter
|
|
|
XM_011511730.1:c.52594C>T
(TTN)
|
XP_011510032.1:p.Gln17532Ter
|
|
|
XM_011511731.1:c.52453C>T
(TTN)
|
XP_011510033.1:p.Gln17485Ter
|
|
|
XM_017004819.1:c.78496C>T
(TTN)
|
XP_016860308.1:p.Gln26166Ter
|
|
|
XM_017004820.1:c.73894C>T
(TTN)
|
XP_016860309.1:p.Gln24632Ter
|
|
|
XM_017004821.1:c.73891C>T
(TTN)
|
XP_016860310.1:p.Gln24631Ter
|
|
|
XM_017004822.1:c.70933C>T
(TTN)
|
XP_016860311.1:p.Gln23645Ter
|
|
|
XM_017004823.1:c.52549C>T
(TTN)
|
XP_016860312.1:p.Gln17517Ter
|
|
|
XM_024453094.1:c.74044C>T
(TTN)
|
XP_024308862.1:p.Gln24682Ter
|
|
|
XM_024453095.1:c.74041C>T
(TTN)
|
XP_024308863.1:p.Gln24681Ter
|
|
|
XM_024453096.1:c.73474C>T
(TTN)
|
XP_024308864.1:p.Gln24492Ter
|
|
|
XM_024453097.1:c.70816C>T
(TTN)
|
XP_024308865.1:p.Gln23606Ter
|
|
|
XM_024453098.1:c.70735C>T
(TTN)
|
XP_024308866.1:p.Gln23579Ter
|
|
|
XM_024453099.1:c.52498C>T
(TTN)
|
XP_024308867.1:p.Gln17500Ter
|
|
|
XM_024453100.1:c.42352C>T
(TTN)
|
XP_024308868.1:p.Gln14118Ter
|
|
