ENST00000342992.11:c.96752A>G
(TTN)
|
ENSP00000343764.6:p.Tyr32251Cys
|
|
ENST00000342175.11:c.77837A>G
(TTN)
|
ENSP00000340554.6:p.Tyr25946Cys
|
|
ENST00000359218.10:c.77636A>G
(TTN)
|
ENSP00000352154.5:p.Tyr25879Cys
|
|
ENST00000342175.10:c.77837A>G
(TTN)
|
ENSP00000340554.6:p.Tyr25946Cys
|
|
ENST00000342992.10:c.96752A>G
(TTN)
|
ENSP00000343764.6:p.Tyr32251Cys
|
|
ENST00000359218.9:c.77636A>G
(TTN)
|
ENSP00000352154.5:p.Tyr25879Cys
|
|
ENST00000460472.6:c.77261A>G
(TTN)
|
ENSP00000434586.1:p.Tyr25754Cys
|
|
ENST00000589042.5:c.104456A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr34819Cys
|
|
ENST00000591111.5:c.99533A>G
(TTN)
|
ENSP00000465570.1:p.Tyr33178Cys
|
|
ENST00000615779.4:c.99533A>G
(TTN)
|
ENSP00000483597.1:p.Tyr33178Cys
|
|
NM_001256850.1:c.99533A>G
(TTN)
|
NP_001243779.1:p.Tyr33178Cys
|
|
NM_001267550.2:c.104456A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr34819Cys
|
|
NM_003319.4:c.77261A>G
(TTN)
|
NP_003310.4:p.Tyr25754Cys
|
|
NM_133378.4:c.96752A>G
(TTN)
|
NP_596869.4:p.Tyr32251Cys
|
|
NM_133432.3:c.77636A>G
(TTN)
|
NP_597676.3:p.Tyr25879Cys
|
|
NM_133437.4:c.77837A>G
(TTN)
|
NP_597681.4:p.Tyr25946Cys
|
|
NR_038271.1:n.446+8523T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3573T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103553A>G
(TTN)
|
XP_011510031.1:p.Tyr34518Cys
|
|
XM_011511730.1:c.77447A>G
(TTN)
|
XP_011510032.1:p.Tyr25816Cys
|
|
XM_011511731.1:c.77306A>G
(TTN)
|
XP_011510033.1:p.Tyr25769Cys
|
|
XM_017004819.1:c.103349A>G
(TTN)
|
XP_016860308.1:p.Tyr34450Cys
|
|
XM_017004820.1:c.98747A>G
(TTN)
|
XP_016860309.1:p.Tyr32916Cys
|
|
XM_017004821.1:c.98744A>G
(TTN)
|
XP_016860310.1:p.Tyr32915Cys
|
|
XM_017004822.1:c.95786A>G
(TTN)
|
XP_016860311.1:p.Tyr31929Cys
|
|
XM_017004823.1:c.77402A>G
(TTN)
|
XP_016860312.1:p.Tyr25801Cys
|
|
XM_024453094.1:c.98897A>G
(TTN)
|
XP_024308862.1:p.Tyr32966Cys
|
|
XM_024453095.1:c.98894A>G
(TTN)
|
XP_024308863.1:p.Tyr32965Cys
|
|
XM_024453096.1:c.98327A>G
(TTN)
|
XP_024308864.1:p.Tyr32776Cys
|
|
XM_024453097.1:c.95669A>G
(TTN)
|
XP_024308865.1:p.Tyr31890Cys
|
|
XM_024453098.1:c.95588A>G
(TTN)
|
XP_024308866.1:p.Tyr31863Cys
|
|
XM_024453099.1:c.77351A>G
(TTN)
|
XP_024308867.1:p.Tyr25784Cys
|
|
XM_024453100.1:c.67205A>G
(TTN)
|
XP_024308868.1:p.Tyr22402Cys
|
|