ENST00000342992.11:c.96761C>G
(TTN)
|
ENSP00000343764.6:p.Ser32254Ter
|
|
ENST00000342175.11:c.77846C>G
(TTN)
|
ENSP00000340554.6:p.Ser25949Ter
|
|
ENST00000359218.10:c.77645C>G
(TTN)
|
ENSP00000352154.5:p.Ser25882Ter
|
|
ENST00000342175.10:c.77846C>G
(TTN)
|
ENSP00000340554.6:p.Ser25949Ter
|
|
ENST00000342992.10:c.96761C>G
(TTN)
|
ENSP00000343764.6:p.Ser32254Ter
|
|
ENST00000359218.9:c.77645C>G
(TTN)
|
ENSP00000352154.5:p.Ser25882Ter
|
|
ENST00000460472.6:c.77270C>G
(TTN)
|
ENSP00000434586.1:p.Ser25757Ter
|
|
ENST00000589042.5:c.104465C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34822Ter
|
|
ENST00000591111.5:c.99542C>G
(TTN)
|
ENSP00000465570.1:p.Ser33181Ter
|
|
ENST00000615779.4:c.99542C>G
(TTN)
|
ENSP00000483597.1:p.Ser33181Ter
|
|
NM_001256850.1:c.99542C>G
(TTN)
|
NP_001243779.1:p.Ser33181Ter
|
|
NM_001267550.2:c.104465C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34822Ter
|
|
NM_003319.4:c.77270C>G
(TTN)
|
NP_003310.4:p.Ser25757Ter
|
|
NM_133378.4:c.96761C>G
(TTN)
|
NP_596869.4:p.Ser32254Ter
|
|
NM_133432.3:c.77645C>G
(TTN)
|
NP_597676.3:p.Ser25882Ter
|
|
NM_133437.4:c.77846C>G
(TTN)
|
NP_597681.4:p.Ser25949Ter
|
|
NR_038271.1:n.446+8514G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3582G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103562C>G
(TTN)
|
XP_011510031.1:p.Ser34521Ter
|
|
XM_011511730.1:c.77456C>G
(TTN)
|
XP_011510032.1:p.Ser25819Ter
|
|
XM_011511731.1:c.77315C>G
(TTN)
|
XP_011510033.1:p.Ser25772Ter
|
|
XM_017004819.1:c.103358C>G
(TTN)
|
XP_016860308.1:p.Ser34453Ter
|
|
XM_017004820.1:c.98756C>G
(TTN)
|
XP_016860309.1:p.Ser32919Ter
|
|
XM_017004821.1:c.98753C>G
(TTN)
|
XP_016860310.1:p.Ser32918Ter
|
|
XM_017004822.1:c.95795C>G
(TTN)
|
XP_016860311.1:p.Ser31932Ter
|
|
XM_017004823.1:c.77411C>G
(TTN)
|
XP_016860312.1:p.Ser25804Ter
|
|
XM_024453094.1:c.98906C>G
(TTN)
|
XP_024308862.1:p.Ser32969Ter
|
|
XM_024453095.1:c.98903C>G
(TTN)
|
XP_024308863.1:p.Ser32968Ter
|
|
XM_024453096.1:c.98336C>G
(TTN)
|
XP_024308864.1:p.Ser32779Ter
|
|
XM_024453097.1:c.95678C>G
(TTN)
|
XP_024308865.1:p.Ser31893Ter
|
|
XM_024453098.1:c.95597C>G
(TTN)
|
XP_024308866.1:p.Ser31866Ter
|
|
XM_024453099.1:c.77360C>G
(TTN)
|
XP_024308867.1:p.Ser25787Ter
|
|
XM_024453100.1:c.67214C>G
(TTN)
|
XP_024308868.1:p.Ser22405Ter
|
|