ENST00000342992.11:c.78590T>G
(TTN)
|
ENSP00000343764.6:p.Ile26197Ser
|
|
ENST00000342175.11:c.59675T>G
(TTN)
|
ENSP00000340554.6:p.Ile19892Ser
|
|
ENST00000359218.10:c.59474T>G
(TTN)
|
ENSP00000352154.5:p.Ile19825Ser
|
|
ENST00000342175.10:c.59675T>G
(TTN)
|
ENSP00000340554.6:p.Ile19892Ser
|
|
ENST00000342992.10:c.78590T>G
(TTN)
|
ENSP00000343764.6:p.Ile26197Ser
|
|
ENST00000359218.9:c.59474T>G
(TTN)
|
ENSP00000352154.5:p.Ile19825Ser
|
|
ENST00000460472.6:c.59099T>G
(TTN)
|
ENSP00000434586.1:p.Ile19700Ser
|
|
ENST00000589042.5:c.86294T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile28765Ser
|
|
ENST00000591111.5:c.81371T>G
(TTN)
|
ENSP00000465570.1:p.Ile27124Ser
|
|
ENST00000615779.4:c.81371T>G
(TTN)
|
ENSP00000483597.1:p.Ile27124Ser
|
|
NM_001256850.1:c.81371T>G
(TTN)
|
NP_001243779.1:p.Ile27124Ser
|
|
NM_001267550.2:c.86294T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ile28765Ser
|
|
NM_003319.4:c.59099T>G
(TTN)
|
NP_003310.4:p.Ile19700Ser
|
|
NM_133378.4:c.78590T>G
(TTN)
|
NP_596869.4:p.Ile26197Ser
|
|
NM_133432.3:c.59474T>G
(TTN)
|
NP_597676.3:p.Ile19825Ser
|
|
NM_133437.4:c.59675T>G
(TTN)
|
NP_597681.4:p.Ile19892Ser
|
|
NR_038271.1:n.447-11462A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17477A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.85391T>G
(TTN)
|
XP_011510031.1:p.Ile28464Ser
|
|
XM_011511730.1:c.59285T>G
(TTN)
|
XP_011510032.1:p.Ile19762Ser
|
|
XM_011511731.1:c.59144T>G
(TTN)
|
XP_011510033.1:p.Ile19715Ser
|
|
XM_017004819.1:c.85187T>G
(TTN)
|
XP_016860308.1:p.Ile28396Ser
|
|
XM_017004820.1:c.80585T>G
(TTN)
|
XP_016860309.1:p.Ile26862Ser
|
|
XM_017004821.1:c.80582T>G
(TTN)
|
XP_016860310.1:p.Ile26861Ser
|
|
XM_017004822.1:c.77624T>G
(TTN)
|
XP_016860311.1:p.Ile25875Ser
|
|
XM_017004823.1:c.59240T>G
(TTN)
|
XP_016860312.1:p.Ile19747Ser
|
|
XM_024453094.1:c.80735T>G
(TTN)
|
XP_024308862.1:p.Ile26912Ser
|
|
XM_024453095.1:c.80732T>G
(TTN)
|
XP_024308863.1:p.Ile26911Ser
|
|
XM_024453096.1:c.80165T>G
(TTN)
|
XP_024308864.1:p.Ile26722Ser
|
|
XM_024453097.1:c.77507T>G
(TTN)
|
XP_024308865.1:p.Ile25836Ser
|
|
XM_024453098.1:c.77426T>G
(TTN)
|
XP_024308866.1:p.Ile25809Ser
|
|
XM_024453099.1:c.59189T>G
(TTN)
|
XP_024308867.1:p.Ile19730Ser
|
|
XM_024453100.1:c.49043T>G
(TTN)
|
XP_024308868.1:p.Ile16348Ser
|
|