ENST00000342992.11:c.68541A>T
(TTN)
|
ENSP00000343764.6:p.Ile22847=
|
|
ENST00000342175.11:c.49626A>T
(TTN)
|
ENSP00000340554.6:p.Ile16542=
|
|
ENST00000359218.10:c.49425A>T
(TTN)
|
ENSP00000352154.5:p.Ile16475=
|
|
ENST00000342175.10:c.49626A>T
(TTN)
|
ENSP00000340554.6:p.Ile16542=
|
|
ENST00000342992.10:c.68541A>T
(TTN)
|
ENSP00000343764.6:p.Ile22847=
|
|
ENST00000359218.9:c.49425A>T
(TTN)
|
ENSP00000352154.5:p.Ile16475=
|
|
ENST00000460472.6:c.49050A>T
(TTN)
|
ENSP00000434586.1:p.Ile16350=
|
|
ENST00000589042.5:c.76245A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile25415=
|
|
ENST00000591111.5:c.71322A>T
(TTN)
|
ENSP00000465570.1:p.Ile23774=
|
|
ENST00000615779.4:c.71322A>T
(TTN)
|
ENSP00000483597.1:p.Ile23774=
|
|
NM_001256850.1:c.71322A>T
(TTN)
|
NP_001243779.1:p.Ile23774=
|
|
NM_001267550.2:c.76245A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ile25415=
|
|
NM_003319.4:c.49050A>T
(TTN)
|
NP_003310.4:p.Ile16350=
|
|
NM_133378.4:c.68541A>T
(TTN)
|
NP_596869.4:p.Ile22847=
|
|
NM_133432.3:c.49425A>T
(TTN)
|
NP_597676.3:p.Ile16475=
|
|
NM_133437.4:c.49626A>T
(TTN)
|
NP_597681.4:p.Ile16542=
|
|
NR_038271.1:n.447-1413T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12685T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.75342A>T
(TTN)
|
XP_011510031.1:p.Ile25114=
|
|
XM_011511730.1:c.49236A>T
(TTN)
|
XP_011510032.1:p.Ile16412=
|
|
XM_011511731.1:c.49095A>T
(TTN)
|
XP_011510033.1:p.Ile16365=
|
|
XM_017004819.1:c.75138A>T
(TTN)
|
XP_016860308.1:p.Ile25046=
|
|
XM_017004820.1:c.70536A>T
(TTN)
|
XP_016860309.1:p.Ile23512=
|
|
XM_017004821.1:c.70533A>T
(TTN)
|
XP_016860310.1:p.Ile23511=
|
|
XM_017004822.1:c.67575A>T
(TTN)
|
XP_016860311.1:p.Ile22525=
|
|
XM_017004823.1:c.49191A>T
(TTN)
|
XP_016860312.1:p.Ile16397=
|
|
XM_024453094.1:c.70686A>T
(TTN)
|
XP_024308862.1:p.Ile23562=
|
|
XM_024453095.1:c.70683A>T
(TTN)
|
XP_024308863.1:p.Ile23561=
|
|
XM_024453096.1:c.70116A>T
(TTN)
|
XP_024308864.1:p.Ile23372=
|
|
XM_024453097.1:c.67458A>T
(TTN)
|
XP_024308865.1:p.Ile22486=
|
|
XM_024453098.1:c.67377A>T
(TTN)
|
XP_024308866.1:p.Ile22459=
|
|
XM_024453099.1:c.49140A>T
(TTN)
|
XP_024308867.1:p.Ile16380=
|
|
XM_024453100.1:c.38994A>T
(TTN)
|
XP_024308868.1:p.Ile12998=
|
|