ENST00000342992.11:c.98694T>C
(TTN)
|
ENSP00000343764.6:p.Tyr32898=
|
|
ENST00000342175.11:c.79779T>C
(TTN)
|
ENSP00000340554.6:p.Tyr26593=
|
|
ENST00000359218.10:c.79578T>C
(TTN)
|
ENSP00000352154.5:p.Tyr26526=
|
|
ENST00000342175.10:c.79779T>C
(TTN)
|
ENSP00000340554.6:p.Tyr26593=
|
|
ENST00000342992.10:c.98694T>C
(TTN)
|
ENSP00000343764.6:p.Tyr32898=
|
|
ENST00000359218.9:c.79578T>C
(TTN)
|
ENSP00000352154.5:p.Tyr26526=
|
|
ENST00000460472.6:c.79203T>C
(TTN)
|
ENSP00000434586.1:p.Tyr26401=
|
|
ENST00000589042.5:c.106398T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr35466=
|
|
ENST00000591111.5:c.101475T>C
(TTN)
|
ENSP00000465570.1:p.Tyr33825=
|
|
ENST00000615779.4:c.101475T>C
(TTN)
|
ENSP00000483597.1:p.Tyr33825=
|
|
NM_001256850.1:c.101475T>C
(TTN)
|
NP_001243779.1:p.Tyr33825=
|
|
NM_001267550.2:c.106398T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr35466=
|
|
NM_003319.4:c.79203T>C
(TTN)
|
NP_003310.4:p.Tyr26401=
|
|
NM_133378.4:c.98694T>C
(TTN)
|
NP_596869.4:p.Tyr32898=
|
|
NM_133432.3:c.79578T>C
(TTN)
|
NP_597676.3:p.Tyr26526=
|
|
NM_133437.4:c.79779T>C
(TTN)
|
NP_597681.4:p.Tyr26593=
|
|
NR_038271.1:n.446+6457A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5639A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105495T>C
(TTN)
|
XP_011510031.1:p.Tyr35165=
|
|
XM_011511730.1:c.79389T>C
(TTN)
|
XP_011510032.1:p.Tyr26463=
|
|
XM_011511731.1:c.79248T>C
(TTN)
|
XP_011510033.1:p.Tyr26416=
|
|
XM_017004819.1:c.105291T>C
(TTN)
|
XP_016860308.1:p.Tyr35097=
|
|
XM_017004820.1:c.100689T>C
(TTN)
|
XP_016860309.1:p.Tyr33563=
|
|
XM_017004821.1:c.100686T>C
(TTN)
|
XP_016860310.1:p.Tyr33562=
|
|
XM_017004822.1:c.97728T>C
(TTN)
|
XP_016860311.1:p.Tyr32576=
|
|
XM_017004823.1:c.79344T>C
(TTN)
|
XP_016860312.1:p.Tyr26448=
|
|
XM_024453094.1:c.100839T>C
(TTN)
|
XP_024308862.1:p.Tyr33613=
|
|
XM_024453095.1:c.100836T>C
(TTN)
|
XP_024308863.1:p.Tyr33612=
|
|
XM_024453096.1:c.100269T>C
(TTN)
|
XP_024308864.1:p.Tyr33423=
|
|
XM_024453097.1:c.97611T>C
(TTN)
|
XP_024308865.1:p.Tyr32537=
|
|
XM_024453098.1:c.97530T>C
(TTN)
|
XP_024308866.1:p.Tyr32510=
|
|
XM_024453099.1:c.79293T>C
(TTN)
|
XP_024308867.1:p.Tyr26431=
|
|
XM_024453100.1:c.69147T>C
(TTN)
|
XP_024308868.1:p.Tyr23049=
|
|