ENST00000342992.11:c.52236A>T
(TTN)
|
ENSP00000343764.6:p.Pro17412=
|
|
ENST00000342175.11:c.33321A>T
(TTN)
|
ENSP00000340554.6:p.Pro11107=
|
|
ENST00000359218.10:c.33120A>T
(TTN)
|
ENSP00000352154.5:p.Pro11040=
|
|
ENST00000342175.10:c.33321A>T
(TTN)
|
ENSP00000340554.6:p.Pro11107=
|
|
ENST00000342992.10:c.52236A>T
(TTN)
|
ENSP00000343764.6:p.Pro17412=
|
|
ENST00000359218.9:c.33120A>T
(TTN)
|
ENSP00000352154.5:p.Pro11040=
|
|
ENST00000460472.6:c.32745A>T
(TTN)
|
ENSP00000434586.1:p.Pro10915=
|
|
ENST00000589042.5:c.59940A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19980=
|
|
ENST00000591111.5:c.55017A>T
(TTN)
|
ENSP00000465570.1:p.Pro18339=
|
|
ENST00000615779.4:c.55017A>T
(TTN)
|
ENSP00000483597.1:p.Pro18339=
|
|
NM_001256850.1:c.55017A>T
(TTN)
|
NP_001243779.1:p.Pro18339=
|
|
NM_001267550.2:c.59940A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19980=
|
|
NM_003319.4:c.32745A>T
(TTN)
|
NP_003310.4:p.Pro10915=
|
|
NM_133378.4:c.52236A>T
(TTN)
|
NP_596869.4:p.Pro17412=
|
|
NM_133432.3:c.33120A>T
(TTN)
|
NP_597676.3:p.Pro11040=
|
|
NM_133437.4:c.33321A>T
(TTN)
|
NP_597681.4:p.Pro11107=
|
|
NR_038271.1:n.597-5717T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+565T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.59037A>T
(TTN)
|
XP_011510031.1:p.Pro19679=
|
|
XM_011511730.1:c.32931A>T
(TTN)
|
XP_011510032.1:p.Pro10977=
|
|
XM_011511731.1:c.32790A>T
(TTN)
|
XP_011510033.1:p.Pro10930=
|
|
XM_017004819.1:c.58833A>T
(TTN)
|
XP_016860308.1:p.Pro19611=
|
|
XM_017004820.1:c.54231A>T
(TTN)
|
XP_016860309.1:p.Pro18077=
|
|
XM_017004821.1:c.54228A>T
(TTN)
|
XP_016860310.1:p.Pro18076=
|
|
XM_017004822.1:c.51270A>T
(TTN)
|
XP_016860311.1:p.Pro17090=
|
|
XM_017004823.1:c.32886A>T
(TTN)
|
XP_016860312.1:p.Pro10962=
|
|
XM_024453094.1:c.54381A>T
(TTN)
|
XP_024308862.1:p.Pro18127=
|
|
XM_024453095.1:c.54378A>T
(TTN)
|
XP_024308863.1:p.Pro18126=
|
|
XM_024453096.1:c.53811A>T
(TTN)
|
XP_024308864.1:p.Pro17937=
|
|
XM_024453097.1:c.51153A>T
(TTN)
|
XP_024308865.1:p.Pro17051=
|
|
XM_024453098.1:c.51072A>T
(TTN)
|
XP_024308866.1:p.Pro17024=
|
|
XM_024453099.1:c.32835A>T
(TTN)
|
XP_024308867.1:p.Pro10945=
|
|
XM_024453100.1:c.22689A>T
(TTN)
|
XP_024308868.1:p.Pro7563=
|
|