ENST00000342992.11:c.88945T>G
(TTN)
|
ENSP00000343764.6:p.Ser29649Ala
|
|
ENST00000342175.11:c.70030T>G
(TTN)
|
ENSP00000340554.6:p.Ser23344Ala
|
|
ENST00000359218.10:c.69829T>G
(TTN)
|
ENSP00000352154.5:p.Ser23277Ala
|
|
ENST00000342175.10:c.70030T>G
(TTN)
|
ENSP00000340554.6:p.Ser23344Ala
|
|
ENST00000342992.10:c.88945T>G
(TTN)
|
ENSP00000343764.6:p.Ser29649Ala
|
|
ENST00000359218.9:c.69829T>G
(TTN)
|
ENSP00000352154.5:p.Ser23277Ala
|
|
ENST00000460472.6:c.69454T>G
(TTN)
|
ENSP00000434586.1:p.Ser23152Ala
|
|
ENST00000589042.5:c.96649T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser32217Ala
|
|
ENST00000591111.5:c.91726T>G
(TTN)
|
ENSP00000465570.1:p.Ser30576Ala
|
|
ENST00000615779.4:c.91726T>G
(TTN)
|
ENSP00000483597.1:p.Ser30576Ala
|
|
NM_001256850.1:c.91726T>G
(TTN)
|
NP_001243779.1:p.Ser30576Ala
|
|
NM_001267550.2:c.96649T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser32217Ala
|
|
NM_003319.4:c.69454T>G
(TTN)
|
NP_003310.4:p.Ser23152Ala
|
|
NM_133378.4:c.88945T>G
(TTN)
|
NP_596869.4:p.Ser29649Ala
|
|
NM_133432.3:c.69829T>G
(TTN)
|
NP_597676.3:p.Ser23277Ala
|
|
NM_133437.4:c.70030T>G
(TTN)
|
NP_597681.4:p.Ser23344Ala
|
|
NR_038271.1:n.446+19688A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+963A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.95746T>G
(TTN)
|
XP_011510031.1:p.Ser31916Ala
|
|
XM_011511730.1:c.69640T>G
(TTN)
|
XP_011510032.1:p.Ser23214Ala
|
|
XM_011511731.1:c.69499T>G
(TTN)
|
XP_011510033.1:p.Ser23167Ala
|
|
XM_017004819.1:c.95542T>G
(TTN)
|
XP_016860308.1:p.Ser31848Ala
|
|
XM_017004820.1:c.90940T>G
(TTN)
|
XP_016860309.1:p.Ser30314Ala
|
|
XM_017004821.1:c.90937T>G
(TTN)
|
XP_016860310.1:p.Ser30313Ala
|
|
XM_017004822.1:c.87979T>G
(TTN)
|
XP_016860311.1:p.Ser29327Ala
|
|
XM_017004823.1:c.69595T>G
(TTN)
|
XP_016860312.1:p.Ser23199Ala
|
|
XM_024453094.1:c.91090T>G
(TTN)
|
XP_024308862.1:p.Ser30364Ala
|
|
XM_024453095.1:c.91087T>G
(TTN)
|
XP_024308863.1:p.Ser30363Ala
|
|
XM_024453096.1:c.90520T>G
(TTN)
|
XP_024308864.1:p.Ser30174Ala
|
|
XM_024453097.1:c.87862T>G
(TTN)
|
XP_024308865.1:p.Ser29288Ala
|
|
XM_024453098.1:c.87781T>G
(TTN)
|
XP_024308866.1:p.Ser29261Ala
|
|
XM_024453099.1:c.69544T>G
(TTN)
|
XP_024308867.1:p.Ser23182Ala
|
|
XM_024453100.1:c.59398T>G
(TTN)
|
XP_024308868.1:p.Ser19800Ala
|
|