ENST00000342992.11:c.84260A>C
(TTN)
|
ENSP00000343764.6:p.Tyr28087Ser
|
|
ENST00000342175.11:c.65345A>C
(TTN)
|
ENSP00000340554.6:p.Tyr21782Ser
|
|
ENST00000359218.10:c.65144A>C
(TTN)
|
ENSP00000352154.5:p.Tyr21715Ser
|
|
ENST00000342175.10:c.65345A>C
(TTN)
|
ENSP00000340554.6:p.Tyr21782Ser
|
|
ENST00000342992.10:c.84260A>C
(TTN)
|
ENSP00000343764.6:p.Tyr28087Ser
|
|
ENST00000359218.9:c.65144A>C
(TTN)
|
ENSP00000352154.5:p.Tyr21715Ser
|
|
ENST00000460472.6:c.64769A>C
(TTN)
|
ENSP00000434586.1:p.Tyr21590Ser
|
|
ENST00000589042.5:c.91964A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr30655Ser
|
|
ENST00000591111.5:c.87041A>C
(TTN)
|
ENSP00000465570.1:p.Tyr29014Ser
|
|
ENST00000615779.4:c.87041A>C
(TTN)
|
ENSP00000483597.1:p.Tyr29014Ser
|
|
NM_001256850.1:c.87041A>C
(TTN)
|
NP_001243779.1:p.Tyr29014Ser
|
|
NM_001267550.2:c.91964A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr30655Ser
|
|
NM_003319.4:c.64769A>C
(TTN)
|
NP_003310.4:p.Tyr21590Ser
|
|
NM_133378.4:c.84260A>C
(TTN)
|
NP_596869.4:p.Tyr28087Ser
|
|
NM_133432.3:c.65144A>C
(TTN)
|
NP_597676.3:p.Tyr21715Ser
|
|
NM_133437.4:c.65345A>C
(TTN)
|
NP_597681.4:p.Tyr21782Ser
|
|
NR_038271.1:n.447-21542T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+7397T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.91061A>C
(TTN)
|
XP_011510031.1:p.Tyr30354Ser
|
|
XM_011511730.1:c.64955A>C
(TTN)
|
XP_011510032.1:p.Tyr21652Ser
|
|
XM_011511731.1:c.64814A>C
(TTN)
|
XP_011510033.1:p.Tyr21605Ser
|
|
XM_017004819.1:c.90857A>C
(TTN)
|
XP_016860308.1:p.Tyr30286Ser
|
|
XM_017004820.1:c.86255A>C
(TTN)
|
XP_016860309.1:p.Tyr28752Ser
|
|
XM_017004821.1:c.86252A>C
(TTN)
|
XP_016860310.1:p.Tyr28751Ser
|
|
XM_017004822.1:c.83294A>C
(TTN)
|
XP_016860311.1:p.Tyr27765Ser
|
|
XM_017004823.1:c.64910A>C
(TTN)
|
XP_016860312.1:p.Tyr21637Ser
|
|
XM_024453094.1:c.86405A>C
(TTN)
|
XP_024308862.1:p.Tyr28802Ser
|
|
XM_024453095.1:c.86402A>C
(TTN)
|
XP_024308863.1:p.Tyr28801Ser
|
|
XM_024453096.1:c.85835A>C
(TTN)
|
XP_024308864.1:p.Tyr28612Ser
|
|
XM_024453097.1:c.83177A>C
(TTN)
|
XP_024308865.1:p.Tyr27726Ser
|
|
XM_024453098.1:c.83096A>C
(TTN)
|
XP_024308866.1:p.Tyr27699Ser
|
|
XM_024453099.1:c.64859A>C
(TTN)
|
XP_024308867.1:p.Tyr21620Ser
|
|
XM_024453100.1:c.54713A>C
(TTN)
|
XP_024308868.1:p.Tyr18238Ser
|
|