ENST00000342992.11:c.39569T>G
(TTN)
|
ENSP00000343764.6:p.Val13190Gly
|
|
ENST00000342175.11:c.20654T>G
(TTN)
|
ENSP00000340554.6:p.Val6885Gly
|
|
ENST00000359218.10:c.20453T>G
(TTN)
|
ENSP00000352154.5:p.Val6818Gly
|
|
ENST00000342175.10:c.20654T>G
(TTN)
|
ENSP00000340554.6:p.Val6885Gly
|
|
ENST00000342992.10:c.39569T>G
(TTN)
|
ENSP00000343764.6:p.Val13190Gly
|
|
ENST00000359218.9:c.20453T>G
(TTN)
|
ENSP00000352154.5:p.Val6818Gly
|
|
ENST00000460472.6:c.20078T>G
(TTN)
|
ENSP00000434586.1:p.Val6693Gly
|
|
ENST00000589042.5:c.47273T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val15758Gly
|
|
ENST00000591111.5:c.42350T>G
(TTN)
|
ENSP00000465570.1:p.Val14117Gly
|
|
ENST00000615779.4:c.42350T>G
(TTN)
|
ENSP00000483597.1:p.Val14117Gly
|
|
NM_001256850.1:c.42350T>G
(TTN)
|
NP_001243779.1:p.Val14117Gly
|
|
NM_001267550.2:c.47273T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val15758Gly
|
|
NM_003319.4:c.20078T>G
(TTN)
|
NP_003310.4:p.Val6693Gly
|
|
NM_133378.4:c.39569T>G
(TTN)
|
NP_596869.4:p.Val13190Gly
|
|
NM_133432.3:c.20453T>G
(TTN)
|
NP_597676.3:p.Val6818Gly
|
|
NM_133437.4:c.20654T>G
(TTN)
|
NP_597681.4:p.Val6885Gly
|
|
NR_038271.1:n.1605-1675A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.46370T>G
(TTN)
|
XP_011510031.1:p.Val15457Gly
|
|
XM_011511730.1:c.20264T>G
(TTN)
|
XP_011510032.1:p.Val6755Gly
|
|
XM_011511731.1:c.20123T>G
(TTN)
|
XP_011510033.1:p.Val6708Gly
|
|
XM_017004819.1:c.46166T>G
(TTN)
|
XP_016860308.1:p.Val15389Gly
|
|
XM_017004820.1:c.41564T>G
(TTN)
|
XP_016860309.1:p.Val13855Gly
|
|
XM_017004821.1:c.41561T>G
(TTN)
|
XP_016860310.1:p.Val13854Gly
|
|
XM_017004822.1:c.38603T>G
(TTN)
|
XP_016860311.1:p.Val12868Gly
|
|
XM_017004823.1:c.20219T>G
(TTN)
|
XP_016860312.1:p.Val6740Gly
|
|
XM_024453094.1:c.41714T>G
(TTN)
|
XP_024308862.1:p.Val13905Gly
|
|
XM_024453095.1:c.41711T>G
(TTN)
|
XP_024308863.1:p.Val13904Gly
|
|
XM_024453096.1:c.41144T>G
(TTN)
|
XP_024308864.1:p.Val13715Gly
|
|
XM_024453097.1:c.38486T>G
(TTN)
|
XP_024308865.1:p.Val12829Gly
|
|
XM_024453098.1:c.38405T>G
(TTN)
|
XP_024308866.1:p.Val12802Gly
|
|
XM_024453099.1:c.20168T>G
(TTN)
|
XP_024308867.1:p.Val6723Gly
|
|
XM_024453100.1:c.10022T>G
(TTN)
|
XP_024308868.1:p.Val3341Gly
|
|