ENST00000342992.11:c.73821T>C
(TTN)
|
ENSP00000343764.6:p.Gly24607=
|
|
ENST00000342175.11:c.54906T>C
(TTN)
|
ENSP00000340554.6:p.Gly18302=
|
|
ENST00000359218.10:c.54705T>C
(TTN)
|
ENSP00000352154.5:p.Gly18235=
|
|
ENST00000342175.10:c.54906T>C
(TTN)
|
ENSP00000340554.6:p.Gly18302=
|
|
ENST00000342992.10:c.73821T>C
(TTN)
|
ENSP00000343764.6:p.Gly24607=
|
|
ENST00000359218.9:c.54705T>C
(TTN)
|
ENSP00000352154.5:p.Gly18235=
|
|
ENST00000460472.6:c.54330T>C
(TTN)
|
ENSP00000434586.1:p.Gly18110=
|
|
ENST00000589042.5:c.81525T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly27175=
|
|
ENST00000591111.5:c.76602T>C
(TTN)
|
ENSP00000465570.1:p.Gly25534=
|
|
ENST00000615779.4:c.76602T>C
(TTN)
|
ENSP00000483597.1:p.Gly25534=
|
|
NM_001256850.1:c.76602T>C
(TTN)
|
NP_001243779.1:p.Gly25534=
|
|
NM_001267550.2:c.81525T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly27175=
|
|
NM_003319.4:c.54330T>C
(TTN)
|
NP_003310.4:p.Gly18110=
|
|
NM_133378.4:c.73821T>C
(TTN)
|
NP_596869.4:p.Gly24607=
|
|
NM_133432.3:c.54705T>C
(TTN)
|
NP_597676.3:p.Gly18235=
|
|
NM_133437.4:c.54906T>C
(TTN)
|
NP_597681.4:p.Gly18302=
|
|
NR_038271.1:n.447-6693A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-17965A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.80622T>C
(TTN)
|
XP_011510031.1:p.Gly26874=
|
|
XM_011511730.1:c.54516T>C
(TTN)
|
XP_011510032.1:p.Gly18172=
|
|
XM_011511731.1:c.54375T>C
(TTN)
|
XP_011510033.1:p.Gly18125=
|
|
XM_017004819.1:c.80418T>C
(TTN)
|
XP_016860308.1:p.Gly26806=
|
|
XM_017004820.1:c.75816T>C
(TTN)
|
XP_016860309.1:p.Gly25272=
|
|
XM_017004821.1:c.75813T>C
(TTN)
|
XP_016860310.1:p.Gly25271=
|
|
XM_017004822.1:c.72855T>C
(TTN)
|
XP_016860311.1:p.Gly24285=
|
|
XM_017004823.1:c.54471T>C
(TTN)
|
XP_016860312.1:p.Gly18157=
|
|
XM_024453094.1:c.75966T>C
(TTN)
|
XP_024308862.1:p.Gly25322=
|
|
XM_024453095.1:c.75963T>C
(TTN)
|
XP_024308863.1:p.Gly25321=
|
|
XM_024453096.1:c.75396T>C
(TTN)
|
XP_024308864.1:p.Gly25132=
|
|
XM_024453097.1:c.72738T>C
(TTN)
|
XP_024308865.1:p.Gly24246=
|
|
XM_024453098.1:c.72657T>C
(TTN)
|
XP_024308866.1:p.Gly24219=
|
|
XM_024453099.1:c.54420T>C
(TTN)
|
XP_024308867.1:p.Gly18140=
|
|
XM_024453100.1:c.44274T>C
(TTN)
|
XP_024308868.1:p.Gly14758=
|
|