ENST00000342992.11:c.98402A>G
(TTN)
|
ENSP00000343764.6:p.Lys32801Arg
|
|
ENST00000342175.11:c.79487A>G
(TTN)
|
ENSP00000340554.6:p.Lys26496Arg
|
|
ENST00000359218.10:c.79286A>G
(TTN)
|
ENSP00000352154.5:p.Lys26429Arg
|
|
ENST00000342175.10:c.79487A>G
(TTN)
|
ENSP00000340554.6:p.Lys26496Arg
|
|
ENST00000342992.10:c.98402A>G
(TTN)
|
ENSP00000343764.6:p.Lys32801Arg
|
|
ENST00000359218.9:c.79286A>G
(TTN)
|
ENSP00000352154.5:p.Lys26429Arg
|
|
ENST00000460472.6:c.78911A>G
(TTN)
|
ENSP00000434586.1:p.Lys26304Arg
|
|
ENST00000589042.5:c.106106A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys35369Arg
|
|
ENST00000591111.5:c.101183A>G
(TTN)
|
ENSP00000465570.1:p.Lys33728Arg
|
|
ENST00000615779.4:c.101183A>G
(TTN)
|
ENSP00000483597.1:p.Lys33728Arg
|
|
NM_001256850.1:c.101183A>G
(TTN)
|
NP_001243779.1:p.Lys33728Arg
|
|
NM_001267550.2:c.106106A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Lys35369Arg
|
|
NM_003319.4:c.78911A>G
(TTN)
|
NP_003310.4:p.Lys26304Arg
|
|
NM_133378.4:c.98402A>G
(TTN)
|
NP_596869.4:p.Lys32801Arg
|
|
NM_133432.3:c.79286A>G
(TTN)
|
NP_597676.3:p.Lys26429Arg
|
|
NM_133437.4:c.79487A>G
(TTN)
|
NP_597681.4:p.Lys26496Arg
|
|
NR_038271.1:n.446+6873T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5223T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105203A>G
(TTN)
|
XP_011510031.1:p.Lys35068Arg
|
|
XM_011511730.1:c.79097A>G
(TTN)
|
XP_011510032.1:p.Lys26366Arg
|
|
XM_011511731.1:c.78956A>G
(TTN)
|
XP_011510033.1:p.Lys26319Arg
|
|
XM_017004819.1:c.104999A>G
(TTN)
|
XP_016860308.1:p.Lys35000Arg
|
|
XM_017004820.1:c.100397A>G
(TTN)
|
XP_016860309.1:p.Lys33466Arg
|
|
XM_017004821.1:c.100394A>G
(TTN)
|
XP_016860310.1:p.Lys33465Arg
|
|
XM_017004822.1:c.97436A>G
(TTN)
|
XP_016860311.1:p.Lys32479Arg
|
|
XM_017004823.1:c.79052A>G
(TTN)
|
XP_016860312.1:p.Lys26351Arg
|
|
XM_024453094.1:c.100547A>G
(TTN)
|
XP_024308862.1:p.Lys33516Arg
|
|
XM_024453095.1:c.100544A>G
(TTN)
|
XP_024308863.1:p.Lys33515Arg
|
|
XM_024453096.1:c.99977A>G
(TTN)
|
XP_024308864.1:p.Lys33326Arg
|
|
XM_024453097.1:c.97319A>G
(TTN)
|
XP_024308865.1:p.Lys32440Arg
|
|
XM_024453098.1:c.97238A>G
(TTN)
|
XP_024308866.1:p.Lys32413Arg
|
|
XM_024453099.1:c.79001A>G
(TTN)
|
XP_024308867.1:p.Lys26334Arg
|
|
XM_024453100.1:c.68855A>G
(TTN)
|
XP_024308868.1:p.Lys22952Arg
|
|