ENST00000342992.11:c.100225T>G
(TTN)
|
ENSP00000343764.6:p.Phe33409Val
|
|
ENST00000342175.11:c.81310T>G
(TTN)
|
ENSP00000340554.6:p.Phe27104Val
|
|
ENST00000359218.10:c.81109T>G
(TTN)
|
ENSP00000352154.5:p.Phe27037Val
|
|
ENST00000342175.10:c.81310T>G
(TTN)
|
ENSP00000340554.6:p.Phe27104Val
|
|
ENST00000342992.10:c.100225T>G
(TTN)
|
ENSP00000343764.6:p.Phe33409Val
|
|
ENST00000359218.9:c.81109T>G
(TTN)
|
ENSP00000352154.5:p.Phe27037Val
|
|
ENST00000460472.6:c.80734T>G
(TTN)
|
ENSP00000434586.1:p.Phe26912Val
|
|
ENST00000589042.5:c.107929T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe35977Val
|
|
ENST00000591111.5:c.103006T>G
(TTN)
|
ENSP00000465570.1:p.Phe34336Val
|
|
ENST00000615779.4:c.103006T>G
(TTN)
|
ENSP00000483597.1:p.Phe34336Val
|
|
NM_001256850.1:c.103006T>G
(TTN)
|
NP_001243779.1:p.Phe34336Val
|
|
NM_001267550.2:c.107929T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Phe35977Val
|
|
NM_003319.4:c.80734T>G
(TTN)
|
NP_003310.4:p.Phe26912Val
|
|
NM_133378.4:c.100225T>G
(TTN)
|
NP_596869.4:p.Phe33409Val
|
|
NM_133432.3:c.81109T>G
(TTN)
|
NP_597676.3:p.Phe27037Val
|
|
NM_133437.4:c.81310T>G
(TTN)
|
NP_597681.4:p.Phe27104Val
|
|
NR_038271.1:n.446+3423A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3423A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.107026T>G
(TTN)
|
XP_011510031.1:p.Phe35676Val
|
|
XM_011511730.1:c.80920T>G
(TTN)
|
XP_011510032.1:p.Phe26974Val
|
|
XM_011511731.1:c.80779T>G
(TTN)
|
XP_011510033.1:p.Phe26927Val
|
|
XM_017004819.1:c.106822T>G
(TTN)
|
XP_016860308.1:p.Phe35608Val
|
|
XM_017004820.1:c.102220T>G
(TTN)
|
XP_016860309.1:p.Phe34074Val
|
|
XM_017004821.1:c.102217T>G
(TTN)
|
XP_016860310.1:p.Phe34073Val
|
|
XM_017004822.1:c.99259T>G
(TTN)
|
XP_016860311.1:p.Phe33087Val
|
|
XM_017004823.1:c.80875T>G
(TTN)
|
XP_016860312.1:p.Phe26959Val
|
|
XM_024453094.1:c.102370T>G
(TTN)
|
XP_024308862.1:p.Phe34124Val
|
|
XM_024453095.1:c.102367T>G
(TTN)
|
XP_024308863.1:p.Phe34123Val
|
|
XM_024453096.1:c.101800T>G
(TTN)
|
XP_024308864.1:p.Phe33934Val
|
|
XM_024453097.1:c.99142T>G
(TTN)
|
XP_024308865.1:p.Phe33048Val
|
|
XM_024453098.1:c.99061T>G
(TTN)
|
XP_024308866.1:p.Phe33021Val
|
|
XM_024453099.1:c.80824T>G
(TTN)
|
XP_024308867.1:p.Phe26942Val
|
|
XM_024453100.1:c.70678T>G
(TTN)
|
XP_024308868.1:p.Phe23560Val
|
|