ENST00000342992.11:c.67191A>C
(TTN)
|
ENSP00000343764.6:p.Gln22397His
|
|
ENST00000342175.11:c.48276A>C
(TTN)
|
ENSP00000340554.6:p.Gln16092His
|
|
ENST00000359218.10:c.48075A>C
(TTN)
|
ENSP00000352154.5:p.Gln16025His
|
|
ENST00000342175.10:c.48276A>C
(TTN)
|
ENSP00000340554.6:p.Gln16092His
|
|
ENST00000342992.10:c.67191A>C
(TTN)
|
ENSP00000343764.6:p.Gln22397His
|
|
ENST00000359218.9:c.48075A>C
(TTN)
|
ENSP00000352154.5:p.Gln16025His
|
|
ENST00000460472.6:c.47700A>C
(TTN)
|
ENSP00000434586.1:p.Gln15900His
|
|
ENST00000589042.5:c.74895A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln24965His
|
|
ENST00000591111.5:c.69972A>C
(TTN)
|
ENSP00000465570.1:p.Gln23324His
|
|
ENST00000615779.4:c.69972A>C
(TTN)
|
ENSP00000483597.1:p.Gln23324His
|
|
NM_001256850.1:c.69972A>C
(TTN)
|
NP_001243779.1:p.Gln23324His
|
|
NM_001267550.2:c.74895A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gln24965His
|
|
NM_003319.4:c.47700A>C
(TTN)
|
NP_003310.4:p.Gln15900His
|
|
NM_133378.4:c.67191A>C
(TTN)
|
NP_596869.4:p.Gln22397His
|
|
NM_133432.3:c.48075A>C
(TTN)
|
NP_597676.3:p.Gln16025His
|
|
NM_133437.4:c.48276A>C
(TTN)
|
NP_597681.4:p.Gln16092His
|
|
NR_038271.1:n.447-63T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-11335T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.73992A>C
(TTN)
|
XP_011510031.1:p.Gln24664His
|
|
XM_011511730.1:c.47886A>C
(TTN)
|
XP_011510032.1:p.Gln15962His
|
|
XM_011511731.1:c.47745A>C
(TTN)
|
XP_011510033.1:p.Gln15915His
|
|
XM_017004819.1:c.73788A>C
(TTN)
|
XP_016860308.1:p.Gln24596His
|
|
XM_017004820.1:c.69186A>C
(TTN)
|
XP_016860309.1:p.Gln23062His
|
|
XM_017004821.1:c.69183A>C
(TTN)
|
XP_016860310.1:p.Gln23061His
|
|
XM_017004822.1:c.66225A>C
(TTN)
|
XP_016860311.1:p.Gln22075His
|
|
XM_017004823.1:c.47841A>C
(TTN)
|
XP_016860312.1:p.Gln15947His
|
|
XM_024453094.1:c.69336A>C
(TTN)
|
XP_024308862.1:p.Gln23112His
|
|
XM_024453095.1:c.69333A>C
(TTN)
|
XP_024308863.1:p.Gln23111His
|
|
XM_024453096.1:c.68766A>C
(TTN)
|
XP_024308864.1:p.Gln22922His
|
|
XM_024453097.1:c.66108A>C
(TTN)
|
XP_024308865.1:p.Gln22036His
|
|
XM_024453098.1:c.66027A>C
(TTN)
|
XP_024308866.1:p.Gln22009His
|
|
XM_024453099.1:c.47790A>C
(TTN)
|
XP_024308867.1:p.Gln15930His
|
|
XM_024453100.1:c.37644A>C
(TTN)
|
XP_024308868.1:p.Gln12548His
|
|