ENST00000342992.11:c.54712G>C
(TTN)
|
ENSP00000343764.6:p.Asp18238His
|
|
ENST00000342175.11:c.35797G>C
(TTN)
|
ENSP00000340554.6:p.Asp11933His
|
|
ENST00000359218.10:c.35596G>C
(TTN)
|
ENSP00000352154.5:p.Asp11866His
|
|
ENST00000342175.10:c.35797G>C
(TTN)
|
ENSP00000340554.6:p.Asp11933His
|
|
ENST00000342992.10:c.54712G>C
(TTN)
|
ENSP00000343764.6:p.Asp18238His
|
|
ENST00000359218.9:c.35596G>C
(TTN)
|
ENSP00000352154.5:p.Asp11866His
|
|
ENST00000460472.6:c.35221G>C
(TTN)
|
ENSP00000434586.1:p.Asp11741His
|
|
ENST00000589042.5:c.62416G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp20806His
|
|
ENST00000591111.5:c.57493G>C
(TTN)
|
ENSP00000465570.1:p.Asp19165His
|
|
ENST00000615779.4:c.57493G>C
(TTN)
|
ENSP00000483597.1:p.Asp19165His
|
|
NM_001256850.1:c.57493G>C
(TTN)
|
NP_001243779.1:p.Asp19165His
|
|
NM_001267550.2:c.62416G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp20806His
|
|
NM_003319.4:c.35221G>C
(TTN)
|
NP_003310.4:p.Asp11741His
|
|
NM_133378.4:c.54712G>C
(TTN)
|
NP_596869.4:p.Asp18238His
|
|
NM_133432.3:c.35596G>C
(TTN)
|
NP_597676.3:p.Asp11866His
|
|
NM_133437.4:c.35797G>C
(TTN)
|
NP_597681.4:p.Asp11933His
|
|
NR_038271.1:n.597-8287C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-1830C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.61513G>C
(TTN)
|
XP_011510031.1:p.Asp20505His
|
|
XM_011511730.1:c.35407G>C
(TTN)
|
XP_011510032.1:p.Asp11803His
|
|
XM_011511731.1:c.35266G>C
(TTN)
|
XP_011510033.1:p.Asp11756His
|
|
XM_017004819.1:c.61309G>C
(TTN)
|
XP_016860308.1:p.Asp20437His
|
|
XM_017004820.1:c.56707G>C
(TTN)
|
XP_016860309.1:p.Asp18903His
|
|
XM_017004821.1:c.56704G>C
(TTN)
|
XP_016860310.1:p.Asp18902His
|
|
XM_017004822.1:c.53746G>C
(TTN)
|
XP_016860311.1:p.Asp17916His
|
|
XM_017004823.1:c.35362G>C
(TTN)
|
XP_016860312.1:p.Asp11788His
|
|
XM_024453094.1:c.56857G>C
(TTN)
|
XP_024308862.1:p.Asp18953His
|
|
XM_024453095.1:c.56854G>C
(TTN)
|
XP_024308863.1:p.Asp18952His
|
|
XM_024453096.1:c.56287G>C
(TTN)
|
XP_024308864.1:p.Asp18763His
|
|
XM_024453097.1:c.53629G>C
(TTN)
|
XP_024308865.1:p.Asp17877His
|
|
XM_024453098.1:c.53548G>C
(TTN)
|
XP_024308866.1:p.Asp17850His
|
|
XM_024453099.1:c.35311G>C
(TTN)
|
XP_024308867.1:p.Asp11771His
|
|
XM_024453100.1:c.25165G>C
(TTN)
|
XP_024308868.1:p.Asp8389His
|
|