ENST00000342992.11:c.88211T>G
(TTN)
|
ENSP00000343764.6:p.Val29404Gly
|
|
ENST00000342175.11:c.69296T>G
(TTN)
|
ENSP00000340554.6:p.Val23099Gly
|
|
ENST00000359218.10:c.69095T>G
(TTN)
|
ENSP00000352154.5:p.Val23032Gly
|
|
ENST00000342175.10:c.69296T>G
(TTN)
|
ENSP00000340554.6:p.Val23099Gly
|
|
ENST00000342992.10:c.88211T>G
(TTN)
|
ENSP00000343764.6:p.Val29404Gly
|
|
ENST00000359218.9:c.69095T>G
(TTN)
|
ENSP00000352154.5:p.Val23032Gly
|
|
ENST00000460472.6:c.68720T>G
(TTN)
|
ENSP00000434586.1:p.Val22907Gly
|
|
ENST00000589042.5:c.95915T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val31972Gly
|
|
ENST00000591111.5:c.90992T>G
(TTN)
|
ENSP00000465570.1:p.Val30331Gly
|
|
ENST00000615779.4:c.90992T>G
(TTN)
|
ENSP00000483597.1:p.Val30331Gly
|
|
NM_001256850.1:c.90992T>G
(TTN)
|
NP_001243779.1:p.Val30331Gly
|
|
NM_001267550.2:c.95915T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val31972Gly
|
|
NM_003319.4:c.68720T>G
(TTN)
|
NP_003310.4:p.Val22907Gly
|
|
NM_133378.4:c.88211T>G
(TTN)
|
NP_596869.4:p.Val29404Gly
|
|
NM_133432.3:c.69095T>G
(TTN)
|
NP_597676.3:p.Val23032Gly
|
|
NM_133437.4:c.69296T>G
(TTN)
|
NP_597681.4:p.Val23099Gly
|
|
NR_038271.1:n.446+20678A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1953A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.95012T>G
(TTN)
|
XP_011510031.1:p.Val31671Gly
|
|
XM_011511730.1:c.68906T>G
(TTN)
|
XP_011510032.1:p.Val22969Gly
|
|
XM_011511731.1:c.68765T>G
(TTN)
|
XP_011510033.1:p.Val22922Gly
|
|
XM_017004819.1:c.94808T>G
(TTN)
|
XP_016860308.1:p.Val31603Gly
|
|
XM_017004820.1:c.90206T>G
(TTN)
|
XP_016860309.1:p.Val30069Gly
|
|
XM_017004821.1:c.90203T>G
(TTN)
|
XP_016860310.1:p.Val30068Gly
|
|
XM_017004822.1:c.87245T>G
(TTN)
|
XP_016860311.1:p.Val29082Gly
|
|
XM_017004823.1:c.68861T>G
(TTN)
|
XP_016860312.1:p.Val22954Gly
|
|
XM_024453094.1:c.90356T>G
(TTN)
|
XP_024308862.1:p.Val30119Gly
|
|
XM_024453095.1:c.90353T>G
(TTN)
|
XP_024308863.1:p.Val30118Gly
|
|
XM_024453096.1:c.89786T>G
(TTN)
|
XP_024308864.1:p.Val29929Gly
|
|
XM_024453097.1:c.87128T>G
(TTN)
|
XP_024308865.1:p.Val29043Gly
|
|
XM_024453098.1:c.87047T>G
(TTN)
|
XP_024308866.1:p.Val29016Gly
|
|
XM_024453099.1:c.68810T>G
(TTN)
|
XP_024308867.1:p.Val22937Gly
|
|
XM_024453100.1:c.58664T>G
(TTN)
|
XP_024308868.1:p.Val19555Gly
|
|