ENST00000342992.11:c.98284G>C
(TTN)
|
ENSP00000343764.6:p.Gly32762Arg
|
|
ENST00000342175.11:c.79369G>C
(TTN)
|
ENSP00000340554.6:p.Gly26457Arg
|
|
ENST00000359218.10:c.79168G>C
(TTN)
|
ENSP00000352154.5:p.Gly26390Arg
|
|
ENST00000342175.10:c.79369G>C
(TTN)
|
ENSP00000340554.6:p.Gly26457Arg
|
|
ENST00000342992.10:c.98284G>C
(TTN)
|
ENSP00000343764.6:p.Gly32762Arg
|
|
ENST00000359218.9:c.79168G>C
(TTN)
|
ENSP00000352154.5:p.Gly26390Arg
|
|
ENST00000460472.6:c.78793G>C
(TTN)
|
ENSP00000434586.1:p.Gly26265Arg
|
|
ENST00000589042.5:c.105988G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35330Arg
|
|
ENST00000591111.5:c.101065G>C
(TTN)
|
ENSP00000465570.1:p.Gly33689Arg
|
|
ENST00000615779.4:c.101065G>C
(TTN)
|
ENSP00000483597.1:p.Gly33689Arg
|
|
NM_001256850.1:c.101065G>C
(TTN)
|
NP_001243779.1:p.Gly33689Arg
|
|
NM_001267550.2:c.105988G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35330Arg
|
|
NM_003319.4:c.78793G>C
(TTN)
|
NP_003310.4:p.Gly26265Arg
|
|
NM_133378.4:c.98284G>C
(TTN)
|
NP_596869.4:p.Gly32762Arg
|
|
NM_133432.3:c.79168G>C
(TTN)
|
NP_597676.3:p.Gly26390Arg
|
|
NM_133437.4:c.79369G>C
(TTN)
|
NP_597681.4:p.Gly26457Arg
|
|
NR_038271.1:n.446+6991C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5105C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105085G>C
(TTN)
|
XP_011510031.1:p.Gly35029Arg
|
|
XM_011511730.1:c.78979G>C
(TTN)
|
XP_011510032.1:p.Gly26327Arg
|
|
XM_011511731.1:c.78838G>C
(TTN)
|
XP_011510033.1:p.Gly26280Arg
|
|
XM_017004819.1:c.104881G>C
(TTN)
|
XP_016860308.1:p.Gly34961Arg
|
|
XM_017004820.1:c.100279G>C
(TTN)
|
XP_016860309.1:p.Gly33427Arg
|
|
XM_017004821.1:c.100276G>C
(TTN)
|
XP_016860310.1:p.Gly33426Arg
|
|
XM_017004822.1:c.97318G>C
(TTN)
|
XP_016860311.1:p.Gly32440Arg
|
|
XM_017004823.1:c.78934G>C
(TTN)
|
XP_016860312.1:p.Gly26312Arg
|
|
XM_024453094.1:c.100429G>C
(TTN)
|
XP_024308862.1:p.Gly33477Arg
|
|
XM_024453095.1:c.100426G>C
(TTN)
|
XP_024308863.1:p.Gly33476Arg
|
|
XM_024453096.1:c.99859G>C
(TTN)
|
XP_024308864.1:p.Gly33287Arg
|
|
XM_024453097.1:c.97201G>C
(TTN)
|
XP_024308865.1:p.Gly32401Arg
|
|
XM_024453098.1:c.97120G>C
(TTN)
|
XP_024308866.1:p.Gly32374Arg
|
|
XM_024453099.1:c.78883G>C
(TTN)
|
XP_024308867.1:p.Gly26295Arg
|
|
XM_024453100.1:c.68737G>C
(TTN)
|
XP_024308868.1:p.Gly22913Arg
|
|