ENST00000342992.11:c.54612T>C
(TTN)
|
ENSP00000343764.6:p.Asp18204=
|
|
ENST00000342175.11:c.35697T>C
(TTN)
|
ENSP00000340554.6:p.Asp11899=
|
|
ENST00000359218.10:c.35496T>C
(TTN)
|
ENSP00000352154.5:p.Asp11832=
|
|
ENST00000342175.10:c.35697T>C
(TTN)
|
ENSP00000340554.6:p.Asp11899=
|
|
ENST00000342992.10:c.54612T>C
(TTN)
|
ENSP00000343764.6:p.Asp18204=
|
|
ENST00000359218.9:c.35496T>C
(TTN)
|
ENSP00000352154.5:p.Asp11832=
|
|
ENST00000460472.6:c.35121T>C
(TTN)
|
ENSP00000434586.1:p.Asp11707=
|
|
ENST00000589042.5:c.62316T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp20772=
|
|
ENST00000591111.5:c.57393T>C
(TTN)
|
ENSP00000465570.1:p.Asp19131=
|
|
ENST00000615779.4:c.57393T>C
(TTN)
|
ENSP00000483597.1:p.Asp19131=
|
|
NM_001256850.1:c.57393T>C
(TTN)
|
NP_001243779.1:p.Asp19131=
|
|
NM_001267550.2:c.62316T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp20772=
|
|
NM_003319.4:c.35121T>C
(TTN)
|
NP_003310.4:p.Asp11707=
|
|
NM_133378.4:c.54612T>C
(TTN)
|
NP_596869.4:p.Asp18204=
|
|
NM_133432.3:c.35496T>C
(TTN)
|
NP_597676.3:p.Asp11832=
|
|
NM_133437.4:c.35697T>C
(TTN)
|
NP_597681.4:p.Asp11899=
|
|
NR_038271.1:n.597-8187A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-1730A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.61413T>C
(TTN)
|
XP_011510031.1:p.Asp20471=
|
|
XM_011511730.1:c.35307T>C
(TTN)
|
XP_011510032.1:p.Asp11769=
|
|
XM_011511731.1:c.35166T>C
(TTN)
|
XP_011510033.1:p.Asp11722=
|
|
XM_017004819.1:c.61209T>C
(TTN)
|
XP_016860308.1:p.Asp20403=
|
|
XM_017004820.1:c.56607T>C
(TTN)
|
XP_016860309.1:p.Asp18869=
|
|
XM_017004821.1:c.56604T>C
(TTN)
|
XP_016860310.1:p.Asp18868=
|
|
XM_017004822.1:c.53646T>C
(TTN)
|
XP_016860311.1:p.Asp17882=
|
|
XM_017004823.1:c.35262T>C
(TTN)
|
XP_016860312.1:p.Asp11754=
|
|
XM_024453094.1:c.56757T>C
(TTN)
|
XP_024308862.1:p.Asp18919=
|
|
XM_024453095.1:c.56754T>C
(TTN)
|
XP_024308863.1:p.Asp18918=
|
|
XM_024453096.1:c.56187T>C
(TTN)
|
XP_024308864.1:p.Asp18729=
|
|
XM_024453097.1:c.53529T>C
(TTN)
|
XP_024308865.1:p.Asp17843=
|
|
XM_024453098.1:c.53448T>C
(TTN)
|
XP_024308866.1:p.Asp17816=
|
|
XM_024453099.1:c.35211T>C
(TTN)
|
XP_024308867.1:p.Asp11737=
|
|
XM_024453100.1:c.25065T>C
(TTN)
|
XP_024308868.1:p.Asp8355=
|
|