ENST00000342992.11:c.69506T>G
(TTN)
|
ENSP00000343764.6:p.Met23169Arg
|
|
ENST00000342175.11:c.50591T>G
(TTN)
|
ENSP00000340554.6:p.Met16864Arg
|
|
ENST00000359218.10:c.50390T>G
(TTN)
|
ENSP00000352154.5:p.Met16797Arg
|
|
ENST00000342175.10:c.50591T>G
(TTN)
|
ENSP00000340554.6:p.Met16864Arg
|
|
ENST00000342992.10:c.69506T>G
(TTN)
|
ENSP00000343764.6:p.Met23169Arg
|
|
ENST00000359218.9:c.50390T>G
(TTN)
|
ENSP00000352154.5:p.Met16797Arg
|
|
ENST00000460472.6:c.50015T>G
(TTN)
|
ENSP00000434586.1:p.Met16672Arg
|
|
ENST00000589042.5:c.77210T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Met25737Arg
|
|
ENST00000591111.5:c.72287T>G
(TTN)
|
ENSP00000465570.1:p.Met24096Arg
|
|
ENST00000615779.4:c.72287T>G
(TTN)
|
ENSP00000483597.1:p.Met24096Arg
|
|
NM_001256850.1:c.72287T>G
(TTN)
|
NP_001243779.1:p.Met24096Arg
|
|
NM_001267550.2:c.77210T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Met25737Arg
|
|
NM_003319.4:c.50015T>G
(TTN)
|
NP_003310.4:p.Met16672Arg
|
|
NM_133378.4:c.69506T>G
(TTN)
|
NP_596869.4:p.Met23169Arg
|
|
NM_133432.3:c.50390T>G
(TTN)
|
NP_597676.3:p.Met16797Arg
|
|
NM_133437.4:c.50591T>G
(TTN)
|
NP_597681.4:p.Met16864Arg
|
|
NR_038271.1:n.447-2378A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13650A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.76307T>G
(TTN)
|
XP_011510031.1:p.Met25436Arg
|
|
XM_011511730.1:c.50201T>G
(TTN)
|
XP_011510032.1:p.Met16734Arg
|
|
XM_011511731.1:c.50060T>G
(TTN)
|
XP_011510033.1:p.Met16687Arg
|
|
XM_017004819.1:c.76103T>G
(TTN)
|
XP_016860308.1:p.Met25368Arg
|
|
XM_017004820.1:c.71501T>G
(TTN)
|
XP_016860309.1:p.Met23834Arg
|
|
XM_017004821.1:c.71498T>G
(TTN)
|
XP_016860310.1:p.Met23833Arg
|
|
XM_017004822.1:c.68540T>G
(TTN)
|
XP_016860311.1:p.Met22847Arg
|
|
XM_017004823.1:c.50156T>G
(TTN)
|
XP_016860312.1:p.Met16719Arg
|
|
XM_024453094.1:c.71651T>G
(TTN)
|
XP_024308862.1:p.Met23884Arg
|
|
XM_024453095.1:c.71648T>G
(TTN)
|
XP_024308863.1:p.Met23883Arg
|
|
XM_024453096.1:c.71081T>G
(TTN)
|
XP_024308864.1:p.Met23694Arg
|
|
XM_024453097.1:c.68423T>G
(TTN)
|
XP_024308865.1:p.Met22808Arg
|
|
XM_024453098.1:c.68342T>G
(TTN)
|
XP_024308866.1:p.Met22781Arg
|
|
XM_024453099.1:c.50105T>G
(TTN)
|
XP_024308867.1:p.Met16702Arg
|
|
XM_024453100.1:c.39959T>G
(TTN)
|
XP_024308868.1:p.Met13320Arg
|
|