ENST00000342992.11:c.47170G>C
(TTN)
|
ENSP00000343764.6:p.Gly15724Arg
|
|
ENST00000342175.11:c.28255G>C
(TTN)
|
ENSP00000340554.6:p.Gly9419Arg
|
|
ENST00000359218.10:c.28054G>C
(TTN)
|
ENSP00000352154.5:p.Gly9352Arg
|
|
ENST00000342175.10:c.28255G>C
(TTN)
|
ENSP00000340554.6:p.Gly9419Arg
|
|
ENST00000342992.10:c.47170G>C
(TTN)
|
ENSP00000343764.6:p.Gly15724Arg
|
|
ENST00000359218.9:c.28054G>C
(TTN)
|
ENSP00000352154.5:p.Gly9352Arg
|
|
ENST00000460472.6:c.27679G>C
(TTN)
|
ENSP00000434586.1:p.Gly9227Arg
|
|
ENST00000589042.5:c.54874G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly18292Arg
|
|
ENST00000591111.5:c.49951G>C
(TTN)
|
ENSP00000465570.1:p.Gly16651Arg
|
|
ENST00000615779.4:c.49951G>C
(TTN)
|
ENSP00000483597.1:p.Gly16651Arg
|
|
NM_001256850.1:c.49951G>C
(TTN)
|
NP_001243779.1:p.Gly16651Arg
|
|
NM_001267550.2:c.54874G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly18292Arg
|
|
NM_003319.4:c.27679G>C
(TTN)
|
NP_003310.4:p.Gly9227Arg
|
|
NM_133378.4:c.47170G>C
(TTN)
|
NP_596869.4:p.Gly15724Arg
|
|
NM_133432.3:c.28054G>C
(TTN)
|
NP_597676.3:p.Gly9352Arg
|
|
NM_133437.4:c.28255G>C
(TTN)
|
NP_597681.4:p.Gly9419Arg
|
|
NR_038271.1:n.682+4847C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+1861C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.53971G>C
(TTN)
|
XP_011510031.1:p.Gly17991Arg
|
|
XM_011511730.1:c.27865G>C
(TTN)
|
XP_011510032.1:p.Gly9289Arg
|
|
XM_011511731.1:c.27724G>C
(TTN)
|
XP_011510033.1:p.Gly9242Arg
|
|
XM_017004819.1:c.53767G>C
(TTN)
|
XP_016860308.1:p.Gly17923Arg
|
|
XM_017004820.1:c.49165G>C
(TTN)
|
XP_016860309.1:p.Gly16389Arg
|
|
XM_017004821.1:c.49162G>C
(TTN)
|
XP_016860310.1:p.Gly16388Arg
|
|
XM_017004822.1:c.46204G>C
(TTN)
|
XP_016860311.1:p.Gly15402Arg
|
|
XM_017004823.1:c.27820G>C
(TTN)
|
XP_016860312.1:p.Gly9274Arg
|
|
XM_024453094.1:c.49315G>C
(TTN)
|
XP_024308862.1:p.Gly16439Arg
|
|
XM_024453095.1:c.49312G>C
(TTN)
|
XP_024308863.1:p.Gly16438Arg
|
|
XM_024453096.1:c.48745G>C
(TTN)
|
XP_024308864.1:p.Gly16249Arg
|
|
XM_024453097.1:c.46087G>C
(TTN)
|
XP_024308865.1:p.Gly15363Arg
|
|
XM_024453098.1:c.46006G>C
(TTN)
|
XP_024308866.1:p.Gly15336Arg
|
|
XM_024453099.1:c.27769G>C
(TTN)
|
XP_024308867.1:p.Gly9257Arg
|
|
XM_024453100.1:c.17623G>C
(TTN)
|
XP_024308868.1:p.Gly5875Arg
|
|