ENST00000342992.11:c.98339A>C
(TTN)
|
ENSP00000343764.6:p.Asn32780Thr
|
|
ENST00000342175.11:c.79424A>C
(TTN)
|
ENSP00000340554.6:p.Asn26475Thr
|
|
ENST00000359218.10:c.79223A>C
(TTN)
|
ENSP00000352154.5:p.Asn26408Thr
|
|
ENST00000342175.10:c.79424A>C
(TTN)
|
ENSP00000340554.6:p.Asn26475Thr
|
|
ENST00000342992.10:c.98339A>C
(TTN)
|
ENSP00000343764.6:p.Asn32780Thr
|
|
ENST00000359218.9:c.79223A>C
(TTN)
|
ENSP00000352154.5:p.Asn26408Thr
|
|
ENST00000460472.6:c.78848A>C
(TTN)
|
ENSP00000434586.1:p.Asn26283Thr
|
|
ENST00000589042.5:c.106043A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn35348Thr
|
|
ENST00000591111.5:c.101120A>C
(TTN)
|
ENSP00000465570.1:p.Asn33707Thr
|
|
ENST00000615779.4:c.101120A>C
(TTN)
|
ENSP00000483597.1:p.Asn33707Thr
|
|
NM_001256850.1:c.101120A>C
(TTN)
|
NP_001243779.1:p.Asn33707Thr
|
|
NM_001267550.2:c.106043A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asn35348Thr
|
|
NM_003319.4:c.78848A>C
(TTN)
|
NP_003310.4:p.Asn26283Thr
|
|
NM_133378.4:c.98339A>C
(TTN)
|
NP_596869.4:p.Asn32780Thr
|
|
NM_133432.3:c.79223A>C
(TTN)
|
NP_597676.3:p.Asn26408Thr
|
|
NM_133437.4:c.79424A>C
(TTN)
|
NP_597681.4:p.Asn26475Thr
|
|
NR_038271.1:n.446+6936T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5160T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105140A>C
(TTN)
|
XP_011510031.1:p.Asn35047Thr
|
|
XM_011511730.1:c.79034A>C
(TTN)
|
XP_011510032.1:p.Asn26345Thr
|
|
XM_011511731.1:c.78893A>C
(TTN)
|
XP_011510033.1:p.Asn26298Thr
|
|
XM_017004819.1:c.104936A>C
(TTN)
|
XP_016860308.1:p.Asn34979Thr
|
|
XM_017004820.1:c.100334A>C
(TTN)
|
XP_016860309.1:p.Asn33445Thr
|
|
XM_017004821.1:c.100331A>C
(TTN)
|
XP_016860310.1:p.Asn33444Thr
|
|
XM_017004822.1:c.97373A>C
(TTN)
|
XP_016860311.1:p.Asn32458Thr
|
|
XM_017004823.1:c.78989A>C
(TTN)
|
XP_016860312.1:p.Asn26330Thr
|
|
XM_024453094.1:c.100484A>C
(TTN)
|
XP_024308862.1:p.Asn33495Thr
|
|
XM_024453095.1:c.100481A>C
(TTN)
|
XP_024308863.1:p.Asn33494Thr
|
|
XM_024453096.1:c.99914A>C
(TTN)
|
XP_024308864.1:p.Asn33305Thr
|
|
XM_024453097.1:c.97256A>C
(TTN)
|
XP_024308865.1:p.Asn32419Thr
|
|
XM_024453098.1:c.97175A>C
(TTN)
|
XP_024308866.1:p.Asn32392Thr
|
|
XM_024453099.1:c.78938A>C
(TTN)
|
XP_024308867.1:p.Asn26313Thr
|
|
XM_024453100.1:c.68792A>C
(TTN)
|
XP_024308868.1:p.Asn22931Thr
|
|