ENST00000342992.11:c.98504C>G
(TTN)
|
ENSP00000343764.6:p.Thr32835Arg
|
|
ENST00000342175.11:c.79589C>G
(TTN)
|
ENSP00000340554.6:p.Thr26530Arg
|
|
ENST00000359218.10:c.79388C>G
(TTN)
|
ENSP00000352154.5:p.Thr26463Arg
|
|
ENST00000342175.10:c.79589C>G
(TTN)
|
ENSP00000340554.6:p.Thr26530Arg
|
|
ENST00000342992.10:c.98504C>G
(TTN)
|
ENSP00000343764.6:p.Thr32835Arg
|
|
ENST00000359218.9:c.79388C>G
(TTN)
|
ENSP00000352154.5:p.Thr26463Arg
|
|
ENST00000460472.6:c.79013C>G
(TTN)
|
ENSP00000434586.1:p.Thr26338Arg
|
|
ENST00000589042.5:c.106208C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35403Arg
|
|
ENST00000591111.5:c.101285C>G
(TTN)
|
ENSP00000465570.1:p.Thr33762Arg
|
|
ENST00000615779.4:c.101285C>G
(TTN)
|
ENSP00000483597.1:p.Thr33762Arg
|
|
NM_001256850.1:c.101285C>G
(TTN)
|
NP_001243779.1:p.Thr33762Arg
|
|
NM_001267550.2:c.106208C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35403Arg
|
|
NM_003319.4:c.79013C>G
(TTN)
|
NP_003310.4:p.Thr26338Arg
|
|
NM_133378.4:c.98504C>G
(TTN)
|
NP_596869.4:p.Thr32835Arg
|
|
NM_133432.3:c.79388C>G
(TTN)
|
NP_597676.3:p.Thr26463Arg
|
|
NM_133437.4:c.79589C>G
(TTN)
|
NP_597681.4:p.Thr26530Arg
|
|
NR_038271.1:n.446+6771G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5325G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105305C>G
(TTN)
|
XP_011510031.1:p.Thr35102Arg
|
|
XM_011511730.1:c.79199C>G
(TTN)
|
XP_011510032.1:p.Thr26400Arg
|
|
XM_011511731.1:c.79058C>G
(TTN)
|
XP_011510033.1:p.Thr26353Arg
|
|
XM_017004819.1:c.105101C>G
(TTN)
|
XP_016860308.1:p.Thr35034Arg
|
|
XM_017004820.1:c.100499C>G
(TTN)
|
XP_016860309.1:p.Thr33500Arg
|
|
XM_017004821.1:c.100496C>G
(TTN)
|
XP_016860310.1:p.Thr33499Arg
|
|
XM_017004822.1:c.97538C>G
(TTN)
|
XP_016860311.1:p.Thr32513Arg
|
|
XM_017004823.1:c.79154C>G
(TTN)
|
XP_016860312.1:p.Thr26385Arg
|
|
XM_024453094.1:c.100649C>G
(TTN)
|
XP_024308862.1:p.Thr33550Arg
|
|
XM_024453095.1:c.100646C>G
(TTN)
|
XP_024308863.1:p.Thr33549Arg
|
|
XM_024453096.1:c.100079C>G
(TTN)
|
XP_024308864.1:p.Thr33360Arg
|
|
XM_024453097.1:c.97421C>G
(TTN)
|
XP_024308865.1:p.Thr32474Arg
|
|
XM_024453098.1:c.97340C>G
(TTN)
|
XP_024308866.1:p.Thr32447Arg
|
|
XM_024453099.1:c.79103C>G
(TTN)
|
XP_024308867.1:p.Thr26368Arg
|
|
XM_024453100.1:c.68957C>G
(TTN)
|
XP_024308868.1:p.Thr22986Arg
|
|