ENST00000342992.11:c.99877G>C
(TTN)
|
ENSP00000343764.6:p.Glu33293Gln
|
|
ENST00000342175.11:c.80962G>C
(TTN)
|
ENSP00000340554.6:p.Glu26988Gln
|
|
ENST00000359218.10:c.80761G>C
(TTN)
|
ENSP00000352154.5:p.Glu26921Gln
|
|
ENST00000342175.10:c.80962G>C
(TTN)
|
ENSP00000340554.6:p.Glu26988Gln
|
|
ENST00000342992.10:c.99877G>C
(TTN)
|
ENSP00000343764.6:p.Glu33293Gln
|
|
ENST00000359218.9:c.80761G>C
(TTN)
|
ENSP00000352154.5:p.Glu26921Gln
|
|
ENST00000460472.6:c.80386G>C
(TTN)
|
ENSP00000434586.1:p.Glu26796Gln
|
|
ENST00000589042.5:c.107581G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35861Gln
|
|
ENST00000591111.5:c.102658G>C
(TTN)
|
ENSP00000465570.1:p.Glu34220Gln
|
|
ENST00000615779.4:c.102658G>C
(TTN)
|
ENSP00000483597.1:p.Glu34220Gln
|
|
NM_001256850.1:c.102658G>C
(TTN)
|
NP_001243779.1:p.Glu34220Gln
|
|
NM_001267550.2:c.107581G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35861Gln
|
|
NM_003319.4:c.80386G>C
(TTN)
|
NP_003310.4:p.Glu26796Gln
|
|
NM_133378.4:c.99877G>C
(TTN)
|
NP_596869.4:p.Glu33293Gln
|
|
NM_133432.3:c.80761G>C
(TTN)
|
NP_597676.3:p.Glu26921Gln
|
|
NM_133437.4:c.80962G>C
(TTN)
|
NP_597681.4:p.Glu26988Gln
|
|
NR_038271.1:n.446+3909C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3909C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.106678G>C
(TTN)
|
XP_011510031.1:p.Glu35560Gln
|
|
XM_011511730.1:c.80572G>C
(TTN)
|
XP_011510032.1:p.Glu26858Gln
|
|
XM_011511731.1:c.80431G>C
(TTN)
|
XP_011510033.1:p.Glu26811Gln
|
|
XM_017004819.1:c.106474G>C
(TTN)
|
XP_016860308.1:p.Glu35492Gln
|
|
XM_017004820.1:c.101872G>C
(TTN)
|
XP_016860309.1:p.Glu33958Gln
|
|
XM_017004821.1:c.101869G>C
(TTN)
|
XP_016860310.1:p.Glu33957Gln
|
|
XM_017004822.1:c.98911G>C
(TTN)
|
XP_016860311.1:p.Glu32971Gln
|
|
XM_017004823.1:c.80527G>C
(TTN)
|
XP_016860312.1:p.Glu26843Gln
|
|
XM_024453094.1:c.102022G>C
(TTN)
|
XP_024308862.1:p.Glu34008Gln
|
|
XM_024453095.1:c.102019G>C
(TTN)
|
XP_024308863.1:p.Glu34007Gln
|
|
XM_024453096.1:c.101452G>C
(TTN)
|
XP_024308864.1:p.Glu33818Gln
|
|
XM_024453097.1:c.98794G>C
(TTN)
|
XP_024308865.1:p.Glu32932Gln
|
|
XM_024453098.1:c.98713G>C
(TTN)
|
XP_024308866.1:p.Glu32905Gln
|
|
XM_024453099.1:c.80476G>C
(TTN)
|
XP_024308867.1:p.Glu26826Gln
|
|
XM_024453100.1:c.70330G>C
(TTN)
|
XP_024308868.1:p.Glu23444Gln
|
|