ENST00000342992.11:c.96905A>C
(TTN)
|
ENSP00000343764.6:p.Asp32302Ala
|
|
ENST00000342175.11:c.77990A>C
(TTN)
|
ENSP00000340554.6:p.Asp25997Ala
|
|
ENST00000359218.10:c.77789A>C
(TTN)
|
ENSP00000352154.5:p.Asp25930Ala
|
|
ENST00000342175.10:c.77990A>C
(TTN)
|
ENSP00000340554.6:p.Asp25997Ala
|
|
ENST00000342992.10:c.96905A>C
(TTN)
|
ENSP00000343764.6:p.Asp32302Ala
|
|
ENST00000359218.9:c.77789A>C
(TTN)
|
ENSP00000352154.5:p.Asp25930Ala
|
|
ENST00000460472.6:c.77414A>C
(TTN)
|
ENSP00000434586.1:p.Asp25805Ala
|
|
ENST00000589042.5:c.104609A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp34870Ala
|
|
ENST00000591111.5:c.99686A>C
(TTN)
|
ENSP00000465570.1:p.Asp33229Ala
|
|
ENST00000615779.4:c.99686A>C
(TTN)
|
ENSP00000483597.1:p.Asp33229Ala
|
|
NM_001256850.1:c.99686A>C
(TTN)
|
NP_001243779.1:p.Asp33229Ala
|
|
NM_001267550.2:c.104609A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp34870Ala
|
|
NM_003319.4:c.77414A>C
(TTN)
|
NP_003310.4:p.Asp25805Ala
|
|
NM_133378.4:c.96905A>C
(TTN)
|
NP_596869.4:p.Asp32302Ala
|
|
NM_133432.3:c.77789A>C
(TTN)
|
NP_597676.3:p.Asp25930Ala
|
|
NM_133437.4:c.77990A>C
(TTN)
|
NP_597681.4:p.Asp25997Ala
|
|
NR_038271.1:n.446+8370T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3726T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103706A>C
(TTN)
|
XP_011510031.1:p.Asp34569Ala
|
|
XM_011511730.1:c.77600A>C
(TTN)
|
XP_011510032.1:p.Asp25867Ala
|
|
XM_011511731.1:c.77459A>C
(TTN)
|
XP_011510033.1:p.Asp25820Ala
|
|
XM_017004819.1:c.103502A>C
(TTN)
|
XP_016860308.1:p.Asp34501Ala
|
|
XM_017004820.1:c.98900A>C
(TTN)
|
XP_016860309.1:p.Asp32967Ala
|
|
XM_017004821.1:c.98897A>C
(TTN)
|
XP_016860310.1:p.Asp32966Ala
|
|
XM_017004822.1:c.95939A>C
(TTN)
|
XP_016860311.1:p.Asp31980Ala
|
|
XM_017004823.1:c.77555A>C
(TTN)
|
XP_016860312.1:p.Asp25852Ala
|
|
XM_024453094.1:c.99050A>C
(TTN)
|
XP_024308862.1:p.Asp33017Ala
|
|
XM_024453095.1:c.99047A>C
(TTN)
|
XP_024308863.1:p.Asp33016Ala
|
|
XM_024453096.1:c.98480A>C
(TTN)
|
XP_024308864.1:p.Asp32827Ala
|
|
XM_024453097.1:c.95822A>C
(TTN)
|
XP_024308865.1:p.Asp31941Ala
|
|
XM_024453098.1:c.95741A>C
(TTN)
|
XP_024308866.1:p.Asp31914Ala
|
|
XM_024453099.1:c.77504A>C
(TTN)
|
XP_024308867.1:p.Asp25835Ala
|
|
XM_024453100.1:c.67358A>C
(TTN)
|
XP_024308868.1:p.Asp22453Ala
|
|