ENST00000342992.11:c.98272C>G
(TTN)
|
ENSP00000343764.6:p.Leu32758Val
|
|
ENST00000342175.11:c.79357C>G
(TTN)
|
ENSP00000340554.6:p.Leu26453Val
|
|
ENST00000359218.10:c.79156C>G
(TTN)
|
ENSP00000352154.5:p.Leu26386Val
|
|
ENST00000342175.10:c.79357C>G
(TTN)
|
ENSP00000340554.6:p.Leu26453Val
|
|
ENST00000342992.10:c.98272C>G
(TTN)
|
ENSP00000343764.6:p.Leu32758Val
|
|
ENST00000359218.9:c.79156C>G
(TTN)
|
ENSP00000352154.5:p.Leu26386Val
|
|
ENST00000460472.6:c.78781C>G
(TTN)
|
ENSP00000434586.1:p.Leu26261Val
|
|
ENST00000589042.5:c.105976C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35326Val
|
|
ENST00000591111.5:c.101053C>G
(TTN)
|
ENSP00000465570.1:p.Leu33685Val
|
|
ENST00000615779.4:c.101053C>G
(TTN)
|
ENSP00000483597.1:p.Leu33685Val
|
|
NM_001256850.1:c.101053C>G
(TTN)
|
NP_001243779.1:p.Leu33685Val
|
|
NM_001267550.2:c.105976C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35326Val
|
|
NM_003319.4:c.78781C>G
(TTN)
|
NP_003310.4:p.Leu26261Val
|
|
NM_133378.4:c.98272C>G
(TTN)
|
NP_596869.4:p.Leu32758Val
|
|
NM_133432.3:c.79156C>G
(TTN)
|
NP_597676.3:p.Leu26386Val
|
|
NM_133437.4:c.79357C>G
(TTN)
|
NP_597681.4:p.Leu26453Val
|
|
NR_038271.1:n.446+7003G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5093G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105073C>G
(TTN)
|
XP_011510031.1:p.Leu35025Val
|
|
XM_011511730.1:c.78967C>G
(TTN)
|
XP_011510032.1:p.Leu26323Val
|
|
XM_011511731.1:c.78826C>G
(TTN)
|
XP_011510033.1:p.Leu26276Val
|
|
XM_017004819.1:c.104869C>G
(TTN)
|
XP_016860308.1:p.Leu34957Val
|
|
XM_017004820.1:c.100267C>G
(TTN)
|
XP_016860309.1:p.Leu33423Val
|
|
XM_017004821.1:c.100264C>G
(TTN)
|
XP_016860310.1:p.Leu33422Val
|
|
XM_017004822.1:c.97306C>G
(TTN)
|
XP_016860311.1:p.Leu32436Val
|
|
XM_017004823.1:c.78922C>G
(TTN)
|
XP_016860312.1:p.Leu26308Val
|
|
XM_024453094.1:c.100417C>G
(TTN)
|
XP_024308862.1:p.Leu33473Val
|
|
XM_024453095.1:c.100414C>G
(TTN)
|
XP_024308863.1:p.Leu33472Val
|
|
XM_024453096.1:c.99847C>G
(TTN)
|
XP_024308864.1:p.Leu33283Val
|
|
XM_024453097.1:c.97189C>G
(TTN)
|
XP_024308865.1:p.Leu32397Val
|
|
XM_024453098.1:c.97108C>G
(TTN)
|
XP_024308866.1:p.Leu32370Val
|
|
XM_024453099.1:c.78871C>G
(TTN)
|
XP_024308867.1:p.Leu26291Val
|
|
XM_024453100.1:c.68725C>G
(TTN)
|
XP_024308868.1:p.Leu22909Val
|
|