ENST00000342992.11:c.98728G>T
(TTN)
|
ENSP00000343764.6:p.Glu32910Ter
|
|
ENST00000342175.11:c.79813G>T
(TTN)
|
ENSP00000340554.6:p.Glu26605Ter
|
|
ENST00000359218.10:c.79612G>T
(TTN)
|
ENSP00000352154.5:p.Glu26538Ter
|
|
ENST00000342175.10:c.79813G>T
(TTN)
|
ENSP00000340554.6:p.Glu26605Ter
|
|
ENST00000342992.10:c.98728G>T
(TTN)
|
ENSP00000343764.6:p.Glu32910Ter
|
|
ENST00000359218.9:c.79612G>T
(TTN)
|
ENSP00000352154.5:p.Glu26538Ter
|
|
ENST00000460472.6:c.79237G>T
(TTN)
|
ENSP00000434586.1:p.Glu26413Ter
|
|
ENST00000589042.5:c.106432G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35478Ter
|
|
ENST00000591111.5:c.101509G>T
(TTN)
|
ENSP00000465570.1:p.Glu33837Ter
|
|
ENST00000615779.4:c.101509G>T
(TTN)
|
ENSP00000483597.1:p.Glu33837Ter
|
|
NM_001256850.1:c.101509G>T
(TTN)
|
NP_001243779.1:p.Glu33837Ter
|
|
NM_001267550.2:c.106432G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35478Ter
|
|
NM_003319.4:c.79237G>T
(TTN)
|
NP_003310.4:p.Glu26413Ter
|
|
NM_133378.4:c.98728G>T
(TTN)
|
NP_596869.4:p.Glu32910Ter
|
|
NM_133432.3:c.79612G>T
(TTN)
|
NP_597676.3:p.Glu26538Ter
|
|
NM_133437.4:c.79813G>T
(TTN)
|
NP_597681.4:p.Glu26605Ter
|
|
NR_038271.1:n.446+6423C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5673C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105529G>T
(TTN)
|
XP_011510031.1:p.Glu35177Ter
|
|
XM_011511730.1:c.79423G>T
(TTN)
|
XP_011510032.1:p.Glu26475Ter
|
|
XM_011511731.1:c.79282G>T
(TTN)
|
XP_011510033.1:p.Glu26428Ter
|
|
XM_017004819.1:c.105325G>T
(TTN)
|
XP_016860308.1:p.Glu35109Ter
|
|
XM_017004820.1:c.100723G>T
(TTN)
|
XP_016860309.1:p.Glu33575Ter
|
|
XM_017004821.1:c.100720G>T
(TTN)
|
XP_016860310.1:p.Glu33574Ter
|
|
XM_017004822.1:c.97762G>T
(TTN)
|
XP_016860311.1:p.Glu32588Ter
|
|
XM_017004823.1:c.79378G>T
(TTN)
|
XP_016860312.1:p.Glu26460Ter
|
|
XM_024453094.1:c.100873G>T
(TTN)
|
XP_024308862.1:p.Glu33625Ter
|
|
XM_024453095.1:c.100870G>T
(TTN)
|
XP_024308863.1:p.Glu33624Ter
|
|
XM_024453096.1:c.100303G>T
(TTN)
|
XP_024308864.1:p.Glu33435Ter
|
|
XM_024453097.1:c.97645G>T
(TTN)
|
XP_024308865.1:p.Glu32549Ter
|
|
XM_024453098.1:c.97564G>T
(TTN)
|
XP_024308866.1:p.Glu32522Ter
|
|
XM_024453099.1:c.79327G>T
(TTN)
|
XP_024308867.1:p.Glu26443Ter
|
|
XM_024453100.1:c.69181G>T
(TTN)
|
XP_024308868.1:p.Glu23061Ter
|
|