ENST00000342992.11:c.98390G>A
(TTN)
|
ENSP00000343764.6:p.Gly32797Asp
|
|
ENST00000342175.11:c.79475G>A
(TTN)
|
ENSP00000340554.6:p.Gly26492Asp
|
|
ENST00000359218.10:c.79274G>A
(TTN)
|
ENSP00000352154.5:p.Gly26425Asp
|
|
ENST00000342175.10:c.79475G>A
(TTN)
|
ENSP00000340554.6:p.Gly26492Asp
|
|
ENST00000342992.10:c.98390G>A
(TTN)
|
ENSP00000343764.6:p.Gly32797Asp
|
|
ENST00000359218.9:c.79274G>A
(TTN)
|
ENSP00000352154.5:p.Gly26425Asp
|
|
ENST00000460472.6:c.78899G>A
(TTN)
|
ENSP00000434586.1:p.Gly26300Asp
|
|
ENST00000589042.5:c.106094G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35365Asp
|
|
ENST00000591111.5:c.101171G>A
(TTN)
|
ENSP00000465570.1:p.Gly33724Asp
|
|
ENST00000615779.4:c.101171G>A
(TTN)
|
ENSP00000483597.1:p.Gly33724Asp
|
|
NM_001256850.1:c.101171G>A
(TTN)
|
NP_001243779.1:p.Gly33724Asp
|
|
NM_001267550.2:c.106094G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35365Asp
|
|
NM_003319.4:c.78899G>A
(TTN)
|
NP_003310.4:p.Gly26300Asp
|
|
NM_133378.4:c.98390G>A
(TTN)
|
NP_596869.4:p.Gly32797Asp
|
|
NM_133432.3:c.79274G>A
(TTN)
|
NP_597676.3:p.Gly26425Asp
|
|
NM_133437.4:c.79475G>A
(TTN)
|
NP_597681.4:p.Gly26492Asp
|
|
NR_038271.1:n.446+6885C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5211C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105191G>A
(TTN)
|
XP_011510031.1:p.Gly35064Asp
|
|
XM_011511730.1:c.79085G>A
(TTN)
|
XP_011510032.1:p.Gly26362Asp
|
|
XM_011511731.1:c.78944G>A
(TTN)
|
XP_011510033.1:p.Gly26315Asp
|
|
XM_017004819.1:c.104987G>A
(TTN)
|
XP_016860308.1:p.Gly34996Asp
|
|
XM_017004820.1:c.100385G>A
(TTN)
|
XP_016860309.1:p.Gly33462Asp
|
|
XM_017004821.1:c.100382G>A
(TTN)
|
XP_016860310.1:p.Gly33461Asp
|
|
XM_017004822.1:c.97424G>A
(TTN)
|
XP_016860311.1:p.Gly32475Asp
|
|
XM_017004823.1:c.79040G>A
(TTN)
|
XP_016860312.1:p.Gly26347Asp
|
|
XM_024453094.1:c.100535G>A
(TTN)
|
XP_024308862.1:p.Gly33512Asp
|
|
XM_024453095.1:c.100532G>A
(TTN)
|
XP_024308863.1:p.Gly33511Asp
|
|
XM_024453096.1:c.99965G>A
(TTN)
|
XP_024308864.1:p.Gly33322Asp
|
|
XM_024453097.1:c.97307G>A
(TTN)
|
XP_024308865.1:p.Gly32436Asp
|
|
XM_024453098.1:c.97226G>A
(TTN)
|
XP_024308866.1:p.Gly32409Asp
|
|
XM_024453099.1:c.78989G>A
(TTN)
|
XP_024308867.1:p.Gly26330Asp
|
|
XM_024453100.1:c.68843G>A
(TTN)
|
XP_024308868.1:p.Gly22948Asp
|
|