ENST00000342992.11:c.98414A>G
(TTN)
|
ENSP00000343764.6:p.Gln32805Arg
|
|
ENST00000342175.11:c.79499A>G
(TTN)
|
ENSP00000340554.6:p.Gln26500Arg
|
|
ENST00000359218.10:c.79298A>G
(TTN)
|
ENSP00000352154.5:p.Gln26433Arg
|
|
ENST00000342175.10:c.79499A>G
(TTN)
|
ENSP00000340554.6:p.Gln26500Arg
|
|
ENST00000342992.10:c.98414A>G
(TTN)
|
ENSP00000343764.6:p.Gln32805Arg
|
|
ENST00000359218.9:c.79298A>G
(TTN)
|
ENSP00000352154.5:p.Gln26433Arg
|
|
ENST00000460472.6:c.78923A>G
(TTN)
|
ENSP00000434586.1:p.Gln26308Arg
|
|
ENST00000589042.5:c.106118A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln35373Arg
|
|
ENST00000591111.5:c.101195A>G
(TTN)
|
ENSP00000465570.1:p.Gln33732Arg
|
|
ENST00000615779.4:c.101195A>G
(TTN)
|
ENSP00000483597.1:p.Gln33732Arg
|
|
NM_001256850.1:c.101195A>G
(TTN)
|
NP_001243779.1:p.Gln33732Arg
|
|
NM_001267550.2:c.106118A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Gln35373Arg
|
|
NM_003319.4:c.78923A>G
(TTN)
|
NP_003310.4:p.Gln26308Arg
|
|
NM_133378.4:c.98414A>G
(TTN)
|
NP_596869.4:p.Gln32805Arg
|
|
NM_133432.3:c.79298A>G
(TTN)
|
NP_597676.3:p.Gln26433Arg
|
|
NM_133437.4:c.79499A>G
(TTN)
|
NP_597681.4:p.Gln26500Arg
|
|
NR_038271.1:n.446+6861T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5235T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105215A>G
(TTN)
|
XP_011510031.1:p.Gln35072Arg
|
|
XM_011511730.1:c.79109A>G
(TTN)
|
XP_011510032.1:p.Gln26370Arg
|
|
XM_011511731.1:c.78968A>G
(TTN)
|
XP_011510033.1:p.Gln26323Arg
|
|
XM_017004819.1:c.105011A>G
(TTN)
|
XP_016860308.1:p.Gln35004Arg
|
|
XM_017004820.1:c.100409A>G
(TTN)
|
XP_016860309.1:p.Gln33470Arg
|
|
XM_017004821.1:c.100406A>G
(TTN)
|
XP_016860310.1:p.Gln33469Arg
|
|
XM_017004822.1:c.97448A>G
(TTN)
|
XP_016860311.1:p.Gln32483Arg
|
|
XM_017004823.1:c.79064A>G
(TTN)
|
XP_016860312.1:p.Gln26355Arg
|
|
XM_024453094.1:c.100559A>G
(TTN)
|
XP_024308862.1:p.Gln33520Arg
|
|
XM_024453095.1:c.100556A>G
(TTN)
|
XP_024308863.1:p.Gln33519Arg
|
|
XM_024453096.1:c.99989A>G
(TTN)
|
XP_024308864.1:p.Gln33330Arg
|
|
XM_024453097.1:c.97331A>G
(TTN)
|
XP_024308865.1:p.Gln32444Arg
|
|
XM_024453098.1:c.97250A>G
(TTN)
|
XP_024308866.1:p.Gln32417Arg
|
|
XM_024453099.1:c.79013A>G
(TTN)
|
XP_024308867.1:p.Gln26338Arg
|
|
XM_024453100.1:c.68867A>G
(TTN)
|
XP_024308868.1:p.Gln22956Arg
|
|