ENST00000342992.11:c.39574G>C
(TTN)
|
ENSP00000343764.6:p.Gly13192Arg
|
|
ENST00000342175.11:c.20659G>C
(TTN)
|
ENSP00000340554.6:p.Gly6887Arg
|
|
ENST00000359218.10:c.20458G>C
(TTN)
|
ENSP00000352154.5:p.Gly6820Arg
|
|
ENST00000342175.10:c.20659G>C
(TTN)
|
ENSP00000340554.6:p.Gly6887Arg
|
|
ENST00000342992.10:c.39574G>C
(TTN)
|
ENSP00000343764.6:p.Gly13192Arg
|
|
ENST00000359218.9:c.20458G>C
(TTN)
|
ENSP00000352154.5:p.Gly6820Arg
|
|
ENST00000460472.6:c.20083G>C
(TTN)
|
ENSP00000434586.1:p.Gly6695Arg
|
|
ENST00000589042.5:c.47278G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly15760Arg
|
|
ENST00000591111.5:c.42355G>C
(TTN)
|
ENSP00000465570.1:p.Gly14119Arg
|
|
ENST00000615779.4:c.42355G>C
(TTN)
|
ENSP00000483597.1:p.Gly14119Arg
|
|
NM_001256850.1:c.42355G>C
(TTN)
|
NP_001243779.1:p.Gly14119Arg
|
|
NM_001267550.2:c.47278G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly15760Arg
|
|
NM_003319.4:c.20083G>C
(TTN)
|
NP_003310.4:p.Gly6695Arg
|
|
NM_133378.4:c.39574G>C
(TTN)
|
NP_596869.4:p.Gly13192Arg
|
|
NM_133432.3:c.20458G>C
(TTN)
|
NP_597676.3:p.Gly6820Arg
|
|
NM_133437.4:c.20659G>C
(TTN)
|
NP_597681.4:p.Gly6887Arg
|
|
NR_038271.1:n.1605-1680C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.46375G>C
(TTN)
|
XP_011510031.1:p.Gly15459Arg
|
|
XM_011511730.1:c.20269G>C
(TTN)
|
XP_011510032.1:p.Gly6757Arg
|
|
XM_011511731.1:c.20128G>C
(TTN)
|
XP_011510033.1:p.Gly6710Arg
|
|
XM_017004819.1:c.46171G>C
(TTN)
|
XP_016860308.1:p.Gly15391Arg
|
|
XM_017004820.1:c.41569G>C
(TTN)
|
XP_016860309.1:p.Gly13857Arg
|
|
XM_017004821.1:c.41566G>C
(TTN)
|
XP_016860310.1:p.Gly13856Arg
|
|
XM_017004822.1:c.38608G>C
(TTN)
|
XP_016860311.1:p.Gly12870Arg
|
|
XM_017004823.1:c.20224G>C
(TTN)
|
XP_016860312.1:p.Gly6742Arg
|
|
XM_024453094.1:c.41719G>C
(TTN)
|
XP_024308862.1:p.Gly13907Arg
|
|
XM_024453095.1:c.41716G>C
(TTN)
|
XP_024308863.1:p.Gly13906Arg
|
|
XM_024453096.1:c.41149G>C
(TTN)
|
XP_024308864.1:p.Gly13717Arg
|
|
XM_024453097.1:c.38491G>C
(TTN)
|
XP_024308865.1:p.Gly12831Arg
|
|
XM_024453098.1:c.38410G>C
(TTN)
|
XP_024308866.1:p.Gly12804Arg
|
|
XM_024453099.1:c.20173G>C
(TTN)
|
XP_024308867.1:p.Gly6725Arg
|
|
XM_024453100.1:c.10027G>C
(TTN)
|
XP_024308868.1:p.Gly3343Arg
|
|