ENST00000342992.11:c.62347C>G
(TTN)
|
ENSP00000343764.6:p.Arg20783Gly
|
|
ENST00000342175.11:c.43432C>G
(TTN)
|
ENSP00000340554.6:p.Arg14478Gly
|
|
ENST00000359218.10:c.43231C>G
(TTN)
|
ENSP00000352154.5:p.Arg14411Gly
|
|
ENST00000342175.10:c.43432C>G
(TTN)
|
ENSP00000340554.6:p.Arg14478Gly
|
|
ENST00000342992.10:c.62347C>G
(TTN)
|
ENSP00000343764.6:p.Arg20783Gly
|
|
ENST00000359218.9:c.43231C>G
(TTN)
|
ENSP00000352154.5:p.Arg14411Gly
|
|
ENST00000460472.6:c.42856C>G
(TTN)
|
ENSP00000434586.1:p.Arg14286Gly
|
|
ENST00000589042.5:c.70051C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg23351Gly
|
|
ENST00000591111.5:c.65128C>G
(TTN)
|
ENSP00000465570.1:p.Arg21710Gly
|
|
ENST00000615779.4:c.65128C>G
(TTN)
|
ENSP00000483597.1:p.Arg21710Gly
|
|
NM_001256850.1:c.65128C>G
(TTN)
|
NP_001243779.1:p.Arg21710Gly
|
|
NM_001267550.2:c.70051C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Arg23351Gly
|
|
NM_003319.4:c.42856C>G
(TTN)
|
NP_003310.4:p.Arg14286Gly
|
|
NM_133378.4:c.62347C>G
(TTN)
|
NP_596869.4:p.Arg20783Gly
|
|
NM_133432.3:c.43231C>G
(TTN)
|
NP_597676.3:p.Arg14411Gly
|
|
NM_133437.4:c.43432C>G
(TTN)
|
NP_597681.4:p.Arg14478Gly
|
|
NR_038271.1:n.596+4632G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-6491G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.69148C>G
(TTN)
|
XP_011510031.1:p.Arg23050Gly
|
|
XM_011511730.1:c.43042C>G
(TTN)
|
XP_011510032.1:p.Arg14348Gly
|
|
XM_011511731.1:c.42901C>G
(TTN)
|
XP_011510033.1:p.Arg14301Gly
|
|
XM_017004819.1:c.68944C>G
(TTN)
|
XP_016860308.1:p.Arg22982Gly
|
|
XM_017004820.1:c.64342C>G
(TTN)
|
XP_016860309.1:p.Arg21448Gly
|
|
XM_017004821.1:c.64339C>G
(TTN)
|
XP_016860310.1:p.Arg21447Gly
|
|
XM_017004822.1:c.61381C>G
(TTN)
|
XP_016860311.1:p.Arg20461Gly
|
|
XM_017004823.1:c.42997C>G
(TTN)
|
XP_016860312.1:p.Arg14333Gly
|
|
XM_024453094.1:c.64492C>G
(TTN)
|
XP_024308862.1:p.Arg21498Gly
|
|
XM_024453095.1:c.64489C>G
(TTN)
|
XP_024308863.1:p.Arg21497Gly
|
|
XM_024453096.1:c.63922C>G
(TTN)
|
XP_024308864.1:p.Arg21308Gly
|
|
XM_024453097.1:c.61264C>G
(TTN)
|
XP_024308865.1:p.Arg20422Gly
|
|
XM_024453098.1:c.61183C>G
(TTN)
|
XP_024308866.1:p.Arg20395Gly
|
|
XM_024453099.1:c.42946C>G
(TTN)
|
XP_024308867.1:p.Arg14316Gly
|
|
XM_024453100.1:c.32800C>G
(TTN)
|
XP_024308868.1:p.Arg10934Gly
|
|