ENST00000342992.11:c.41654C>A
(TTN)
|
ENSP00000343764.6:p.Pro13885His
|
|
ENST00000342175.11:c.22739C>A
(TTN)
|
ENSP00000340554.6:p.Pro7580His
|
|
ENST00000359218.10:c.22538C>A
(TTN)
|
ENSP00000352154.5:p.Pro7513His
|
|
ENST00000342175.10:c.22739C>A
(TTN)
|
ENSP00000340554.6:p.Pro7580His
|
|
ENST00000342992.10:c.41654C>A
(TTN)
|
ENSP00000343764.6:p.Pro13885His
|
|
ENST00000359218.9:c.22538C>A
(TTN)
|
ENSP00000352154.5:p.Pro7513His
|
|
ENST00000460472.6:c.22163C>A
(TTN)
|
ENSP00000434586.1:p.Pro7388His
|
|
ENST00000589042.5:c.49358C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro16453His
|
|
ENST00000591111.5:c.44435C>A
(TTN)
|
ENSP00000465570.1:p.Pro14812His
|
|
ENST00000615779.4:c.44435C>A
(TTN)
|
ENSP00000483597.1:p.Pro14812His
|
|
NM_001256850.1:c.44435C>A
(TTN)
|
NP_001243779.1:p.Pro14812His
|
|
NM_001267550.2:c.49358C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro16453His
|
|
NM_003319.4:c.22163C>A
(TTN)
|
NP_003310.4:p.Pro7388His
|
|
NM_133378.4:c.41654C>A
(TTN)
|
NP_596869.4:p.Pro13885His
|
|
NM_133432.3:c.22538C>A
(TTN)
|
NP_597676.3:p.Pro7513His
|
|
NM_133437.4:c.22739C>A
(TTN)
|
NP_597681.4:p.Pro7580His
|
|
NR_038271.1:n.783-110G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.48455C>A
(TTN)
|
XP_011510031.1:p.Pro16152His
|
|
XM_011511730.1:c.22349C>A
(TTN)
|
XP_011510032.1:p.Pro7450His
|
|
XM_011511731.1:c.22208C>A
(TTN)
|
XP_011510033.1:p.Pro7403His
|
|
XM_017004819.1:c.48251C>A
(TTN)
|
XP_016860308.1:p.Pro16084His
|
|
XM_017004820.1:c.43649C>A
(TTN)
|
XP_016860309.1:p.Pro14550His
|
|
XM_017004821.1:c.43646C>A
(TTN)
|
XP_016860310.1:p.Pro14549His
|
|
XM_017004822.1:c.40688C>A
(TTN)
|
XP_016860311.1:p.Pro13563His
|
|
XM_017004823.1:c.22304C>A
(TTN)
|
XP_016860312.1:p.Pro7435His
|
|
XM_024453094.1:c.43799C>A
(TTN)
|
XP_024308862.1:p.Pro14600His
|
|
XM_024453095.1:c.43796C>A
(TTN)
|
XP_024308863.1:p.Pro14599His
|
|
XM_024453096.1:c.43229C>A
(TTN)
|
XP_024308864.1:p.Pro14410His
|
|
XM_024453097.1:c.40571C>A
(TTN)
|
XP_024308865.1:p.Pro13524His
|
|
XM_024453098.1:c.40490C>A
(TTN)
|
XP_024308866.1:p.Pro13497His
|
|
XM_024453099.1:c.22253C>A
(TTN)
|
XP_024308867.1:p.Pro7418His
|
|
XM_024453100.1:c.12107C>A
(TTN)
|
XP_024308868.1:p.Pro4036His
|
|