|
ENST00000342992.11:c.70700G>A
(TTN)
|
ENSP00000343764.6:p.Trp23567Ter
|
|
|
ENST00000342175.11:c.51785G>A
(TTN)
|
ENSP00000340554.6:p.Trp17262Ter
|
|
|
ENST00000359218.10:c.51584G>A
(TTN)
|
ENSP00000352154.5:p.Trp17195Ter
|
|
|
ENST00000342175.10:c.51785G>A
(TTN)
|
ENSP00000340554.6:p.Trp17262Ter
|
|
|
ENST00000342992.10:c.70700G>A
(TTN)
|
ENSP00000343764.6:p.Trp23567Ter
|
|
|
ENST00000359218.9:c.51584G>A
(TTN)
|
ENSP00000352154.5:p.Trp17195Ter
|
|
|
ENST00000460472.6:c.51209G>A
(TTN)
|
ENSP00000434586.1:p.Trp17070Ter
|
|
|
ENST00000589042.5:c.78404G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Trp26135Ter
|
|
|
ENST00000591111.5:c.73481G>A
(TTN)
|
ENSP00000465570.1:p.Trp24494Ter
|
|
|
ENST00000615779.4:c.73481G>A
(TTN)
|
ENSP00000483597.1:p.Trp24494Ter
|
|
|
NM_001256850.1:c.73481G>A
(TTN)
|
NP_001243779.1:p.Trp24494Ter
|
|
|
NM_001267550.2:c.78404G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Trp26135Ter
|
|
|
NM_003319.4:c.51209G>A
(TTN)
|
NP_003310.4:p.Trp17070Ter
|
|
|
NM_133378.4:c.70700G>A
(TTN)
|
NP_596869.4:p.Trp23567Ter
|
|
|
NM_133432.3:c.51584G>A
(TTN)
|
NP_597676.3:p.Trp17195Ter
|
|
|
NM_133437.4:c.51785G>A
(TTN)
|
NP_597681.4:p.Trp17262Ter
|
|
|
NR_038271.1:n.447-3572C>T
(TTN-AS1)
|
|
|
|
NR_038272.1:n.2044-14844C>T
(TTN-AS1)
|
|
|
|
XM_011511729.1:c.77501G>A
(TTN)
|
XP_011510031.1:p.Trp25834Ter
|
|
|
XM_011511730.1:c.51395G>A
(TTN)
|
XP_011510032.1:p.Trp17132Ter
|
|
|
XM_011511731.1:c.51254G>A
(TTN)
|
XP_011510033.1:p.Trp17085Ter
|
|
|
XM_017004819.1:c.77297G>A
(TTN)
|
XP_016860308.1:p.Trp25766Ter
|
|
|
XM_017004820.1:c.72695G>A
(TTN)
|
XP_016860309.1:p.Trp24232Ter
|
|
|
XM_017004821.1:c.72692G>A
(TTN)
|
XP_016860310.1:p.Trp24231Ter
|
|
|
XM_017004822.1:c.69734G>A
(TTN)
|
XP_016860311.1:p.Trp23245Ter
|
|
|
XM_017004823.1:c.51350G>A
(TTN)
|
XP_016860312.1:p.Trp17117Ter
|
|
|
XM_024453094.1:c.72845G>A
(TTN)
|
XP_024308862.1:p.Trp24282Ter
|
|
|
XM_024453095.1:c.72842G>A
(TTN)
|
XP_024308863.1:p.Trp24281Ter
|
|
|
XM_024453096.1:c.72275G>A
(TTN)
|
XP_024308864.1:p.Trp24092Ter
|
|
|
XM_024453097.1:c.69617G>A
(TTN)
|
XP_024308865.1:p.Trp23206Ter
|
|
|
XM_024453098.1:c.69536G>A
(TTN)
|
XP_024308866.1:p.Trp23179Ter
|
|
|
XM_024453099.1:c.51299G>A
(TTN)
|
XP_024308867.1:p.Trp17100Ter
|
|
|
XM_024453100.1:c.41153G>A
(TTN)
|
XP_024308868.1:p.Trp13718Ter
|
|
