ENST00000342992.11:c.69684T>C
(TTN)
|
ENSP00000343764.6:p.Ile23228=
|
|
ENST00000342175.11:c.50769T>C
(TTN)
|
ENSP00000340554.6:p.Ile16923=
|
|
ENST00000359218.10:c.50568T>C
(TTN)
|
ENSP00000352154.5:p.Ile16856=
|
|
ENST00000342175.10:c.50769T>C
(TTN)
|
ENSP00000340554.6:p.Ile16923=
|
|
ENST00000342992.10:c.69684T>C
(TTN)
|
ENSP00000343764.6:p.Ile23228=
|
|
ENST00000359218.9:c.50568T>C
(TTN)
|
ENSP00000352154.5:p.Ile16856=
|
|
ENST00000460472.6:c.50193T>C
(TTN)
|
ENSP00000434586.1:p.Ile16731=
|
|
ENST00000589042.5:c.77388T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile25796=
|
|
ENST00000591111.5:c.72465T>C
(TTN)
|
ENSP00000465570.1:p.Ile24155=
|
|
ENST00000615779.4:c.72465T>C
(TTN)
|
ENSP00000483597.1:p.Ile24155=
|
|
NM_001256850.1:c.72465T>C
(TTN)
|
NP_001243779.1:p.Ile24155=
|
|
NM_001267550.2:c.77388T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ile25796=
|
|
NM_003319.4:c.50193T>C
(TTN)
|
NP_003310.4:p.Ile16731=
|
|
NM_133378.4:c.69684T>C
(TTN)
|
NP_596869.4:p.Ile23228=
|
|
NM_133432.3:c.50568T>C
(TTN)
|
NP_597676.3:p.Ile16856=
|
|
NM_133437.4:c.50769T>C
(TTN)
|
NP_597681.4:p.Ile16923=
|
|
NR_038271.1:n.447-2556A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13828A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.76485T>C
(TTN)
|
XP_011510031.1:p.Ile25495=
|
|
XM_011511730.1:c.50379T>C
(TTN)
|
XP_011510032.1:p.Ile16793=
|
|
XM_011511731.1:c.50238T>C
(TTN)
|
XP_011510033.1:p.Ile16746=
|
|
XM_017004819.1:c.76281T>C
(TTN)
|
XP_016860308.1:p.Ile25427=
|
|
XM_017004820.1:c.71679T>C
(TTN)
|
XP_016860309.1:p.Ile23893=
|
|
XM_017004821.1:c.71676T>C
(TTN)
|
XP_016860310.1:p.Ile23892=
|
|
XM_017004822.1:c.68718T>C
(TTN)
|
XP_016860311.1:p.Ile22906=
|
|
XM_017004823.1:c.50334T>C
(TTN)
|
XP_016860312.1:p.Ile16778=
|
|
XM_024453094.1:c.71829T>C
(TTN)
|
XP_024308862.1:p.Ile23943=
|
|
XM_024453095.1:c.71826T>C
(TTN)
|
XP_024308863.1:p.Ile23942=
|
|
XM_024453096.1:c.71259T>C
(TTN)
|
XP_024308864.1:p.Ile23753=
|
|
XM_024453097.1:c.68601T>C
(TTN)
|
XP_024308865.1:p.Ile22867=
|
|
XM_024453098.1:c.68520T>C
(TTN)
|
XP_024308866.1:p.Ile22840=
|
|
XM_024453099.1:c.50283T>C
(TTN)
|
XP_024308867.1:p.Ile16761=
|
|
XM_024453100.1:c.40137T>C
(TTN)
|
XP_024308868.1:p.Ile13379=
|
|