ENST00000342992.11:c.88980C>G
(TTN)
|
ENSP00000343764.6:p.Tyr29660Ter
|
|
ENST00000342175.11:c.70065C>G
(TTN)
|
ENSP00000340554.6:p.Tyr23355Ter
|
|
ENST00000359218.10:c.69864C>G
(TTN)
|
ENSP00000352154.5:p.Tyr23288Ter
|
|
ENST00000342175.10:c.70065C>G
(TTN)
|
ENSP00000340554.6:p.Tyr23355Ter
|
|
ENST00000342992.10:c.88980C>G
(TTN)
|
ENSP00000343764.6:p.Tyr29660Ter
|
|
ENST00000359218.9:c.69864C>G
(TTN)
|
ENSP00000352154.5:p.Tyr23288Ter
|
|
ENST00000460472.6:c.69489C>G
(TTN)
|
ENSP00000434586.1:p.Tyr23163Ter
|
|
ENST00000589042.5:c.96684C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr32228Ter
|
|
ENST00000591111.5:c.91761C>G
(TTN)
|
ENSP00000465570.1:p.Tyr30587Ter
|
|
ENST00000615779.4:c.91761C>G
(TTN)
|
ENSP00000483597.1:p.Tyr30587Ter
|
|
NM_001256850.1:c.91761C>G
(TTN)
|
NP_001243779.1:p.Tyr30587Ter
|
|
NM_001267550.2:c.96684C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr32228Ter
|
|
NM_003319.4:c.69489C>G
(TTN)
|
NP_003310.4:p.Tyr23163Ter
|
|
NM_133378.4:c.88980C>G
(TTN)
|
NP_596869.4:p.Tyr29660Ter
|
|
NM_133432.3:c.69864C>G
(TTN)
|
NP_597676.3:p.Tyr23288Ter
|
|
NM_133437.4:c.70065C>G
(TTN)
|
NP_597681.4:p.Tyr23355Ter
|
|
NR_038271.1:n.446+19653G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+928G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.95781C>G
(TTN)
|
XP_011510031.1:p.Tyr31927Ter
|
|
XM_011511730.1:c.69675C>G
(TTN)
|
XP_011510032.1:p.Tyr23225Ter
|
|
XM_011511731.1:c.69534C>G
(TTN)
|
XP_011510033.1:p.Tyr23178Ter
|
|
XM_017004819.1:c.95577C>G
(TTN)
|
XP_016860308.1:p.Tyr31859Ter
|
|
XM_017004820.1:c.90975C>G
(TTN)
|
XP_016860309.1:p.Tyr30325Ter
|
|
XM_017004821.1:c.90972C>G
(TTN)
|
XP_016860310.1:p.Tyr30324Ter
|
|
XM_017004822.1:c.88014C>G
(TTN)
|
XP_016860311.1:p.Tyr29338Ter
|
|
XM_017004823.1:c.69630C>G
(TTN)
|
XP_016860312.1:p.Tyr23210Ter
|
|
XM_024453094.1:c.91125C>G
(TTN)
|
XP_024308862.1:p.Tyr30375Ter
|
|
XM_024453095.1:c.91122C>G
(TTN)
|
XP_024308863.1:p.Tyr30374Ter
|
|
XM_024453096.1:c.90555C>G
(TTN)
|
XP_024308864.1:p.Tyr30185Ter
|
|
XM_024453097.1:c.87897C>G
(TTN)
|
XP_024308865.1:p.Tyr29299Ter
|
|
XM_024453098.1:c.87816C>G
(TTN)
|
XP_024308866.1:p.Tyr29272Ter
|
|
XM_024453099.1:c.69579C>G
(TTN)
|
XP_024308867.1:p.Tyr23193Ter
|
|
XM_024453100.1:c.59433C>G
(TTN)
|
XP_024308868.1:p.Tyr19811Ter
|
|