ENST00000342992.11:c.46489C>T
(TTN)
|
ENSP00000343764.6:p.Arg15497Cys
|
|
ENST00000342175.11:c.27574C>T
(TTN)
|
ENSP00000340554.6:p.Arg9192Cys
|
|
ENST00000359218.10:c.27373C>T
(TTN)
|
ENSP00000352154.5:p.Arg9125Cys
|
|
ENST00000342175.10:c.27574C>T
(TTN)
|
ENSP00000340554.6:p.Arg9192Cys
|
|
ENST00000342992.10:c.46489C>T
(TTN)
|
ENSP00000343764.6:p.Arg15497Cys
|
|
ENST00000359218.9:c.27373C>T
(TTN)
|
ENSP00000352154.5:p.Arg9125Cys
|
|
ENST00000460472.6:c.26998C>T
(TTN)
|
ENSP00000434586.1:p.Arg9000Cys
|
|
ENST00000589042.5:c.54193C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg18065Cys
|
|
ENST00000591111.5:c.49270C>T
(TTN)
|
ENSP00000465570.1:p.Arg16424Cys
|
|
ENST00000615779.4:c.49270C>T
(TTN)
|
ENSP00000483597.1:p.Arg16424Cys
|
|
NM_001256850.1:c.49270C>T
(TTN)
|
NP_001243779.1:p.Arg16424Cys
|
|
NM_001267550.2:c.54193C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Arg18065Cys
|
|
NM_003319.4:c.26998C>T
(TTN)
|
NP_003310.4:p.Arg9000Cys
|
|
NM_133378.4:c.46489C>T
(TTN)
|
NP_596869.4:p.Arg15497Cys
|
|
NM_133432.3:c.27373C>T
(TTN)
|
NP_597676.3:p.Arg9125Cys
|
|
NM_133437.4:c.27574C>T
(TTN)
|
NP_597681.4:p.Arg9192Cys
|
|
NR_038271.1:n.683-3271G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.4083G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.53290C>T
(TTN)
|
XP_011510031.1:p.Arg17764Cys
|
|
XM_011511730.1:c.27184C>T
(TTN)
|
XP_011510032.1:p.Arg9062Cys
|
|
XM_011511731.1:c.27043C>T
(TTN)
|
XP_011510033.1:p.Arg9015Cys
|
|
XM_017004819.1:c.53086C>T
(TTN)
|
XP_016860308.1:p.Arg17696Cys
|
|
XM_017004820.1:c.48484C>T
(TTN)
|
XP_016860309.1:p.Arg16162Cys
|
|
XM_017004821.1:c.48481C>T
(TTN)
|
XP_016860310.1:p.Arg16161Cys
|
|
XM_017004822.1:c.45523C>T
(TTN)
|
XP_016860311.1:p.Arg15175Cys
|
|
XM_017004823.1:c.27139C>T
(TTN)
|
XP_016860312.1:p.Arg9047Cys
|
|
XM_024453094.1:c.48634C>T
(TTN)
|
XP_024308862.1:p.Arg16212Cys
|
|
XM_024453095.1:c.48631C>T
(TTN)
|
XP_024308863.1:p.Arg16211Cys
|
|
XM_024453096.1:c.48064C>T
(TTN)
|
XP_024308864.1:p.Arg16022Cys
|
|
XM_024453097.1:c.45406C>T
(TTN)
|
XP_024308865.1:p.Arg15136Cys
|
|
XM_024453098.1:c.45325C>T
(TTN)
|
XP_024308866.1:p.Arg15109Cys
|
|
XM_024453099.1:c.27088C>T
(TTN)
|
XP_024308867.1:p.Arg9030Cys
|
|
XM_024453100.1:c.16942C>T
(TTN)
|
XP_024308868.1:p.Arg5648Cys
|
|