ENST00000342992.11:c.100223A>T
(TTN)
|
ENSP00000343764.6:p.Glu33408Val
|
|
ENST00000342175.11:c.81308A>T
(TTN)
|
ENSP00000340554.6:p.Glu27103Val
|
|
ENST00000359218.10:c.81107A>T
(TTN)
|
ENSP00000352154.5:p.Glu27036Val
|
|
ENST00000342175.10:c.81308A>T
(TTN)
|
ENSP00000340554.6:p.Glu27103Val
|
|
ENST00000342992.10:c.100223A>T
(TTN)
|
ENSP00000343764.6:p.Glu33408Val
|
|
ENST00000359218.9:c.81107A>T
(TTN)
|
ENSP00000352154.5:p.Glu27036Val
|
|
ENST00000460472.6:c.80732A>T
(TTN)
|
ENSP00000434586.1:p.Glu26911Val
|
|
ENST00000589042.5:c.107927A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35976Val
|
|
ENST00000591111.5:c.103004A>T
(TTN)
|
ENSP00000465570.1:p.Glu34335Val
|
|
ENST00000615779.4:c.103004A>T
(TTN)
|
ENSP00000483597.1:p.Glu34335Val
|
|
NM_001256850.1:c.103004A>T
(TTN)
|
NP_001243779.1:p.Glu34335Val
|
|
NM_001267550.2:c.107927A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35976Val
|
|
NM_003319.4:c.80732A>T
(TTN)
|
NP_003310.4:p.Glu26911Val
|
|
NM_133378.4:c.100223A>T
(TTN)
|
NP_596869.4:p.Glu33408Val
|
|
NM_133432.3:c.81107A>T
(TTN)
|
NP_597676.3:p.Glu27036Val
|
|
NM_133437.4:c.81308A>T
(TTN)
|
NP_597681.4:p.Glu27103Val
|
|
NR_038271.1:n.446+3425T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3425T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.107024A>T
(TTN)
|
XP_011510031.1:p.Glu35675Val
|
|
XM_011511730.1:c.80918A>T
(TTN)
|
XP_011510032.1:p.Glu26973Val
|
|
XM_011511731.1:c.80777A>T
(TTN)
|
XP_011510033.1:p.Glu26926Val
|
|
XM_017004819.1:c.106820A>T
(TTN)
|
XP_016860308.1:p.Glu35607Val
|
|
XM_017004820.1:c.102218A>T
(TTN)
|
XP_016860309.1:p.Glu34073Val
|
|
XM_017004821.1:c.102215A>T
(TTN)
|
XP_016860310.1:p.Glu34072Val
|
|
XM_017004822.1:c.99257A>T
(TTN)
|
XP_016860311.1:p.Glu33086Val
|
|
XM_017004823.1:c.80873A>T
(TTN)
|
XP_016860312.1:p.Glu26958Val
|
|
XM_024453094.1:c.102368A>T
(TTN)
|
XP_024308862.1:p.Glu34123Val
|
|
XM_024453095.1:c.102365A>T
(TTN)
|
XP_024308863.1:p.Glu34122Val
|
|
XM_024453096.1:c.101798A>T
(TTN)
|
XP_024308864.1:p.Glu33933Val
|
|
XM_024453097.1:c.99140A>T
(TTN)
|
XP_024308865.1:p.Glu33047Val
|
|
XM_024453098.1:c.99059A>T
(TTN)
|
XP_024308866.1:p.Glu33020Val
|
|
XM_024453099.1:c.80822A>T
(TTN)
|
XP_024308867.1:p.Glu26941Val
|
|
XM_024453100.1:c.70676A>T
(TTN)
|
XP_024308868.1:p.Glu23559Val
|
|