ENST00000342992.11:c.96705A>G
(TTN)
|
ENSP00000343764.6:p.Ser32235=
|
|
ENST00000342175.11:c.77790A>G
(TTN)
|
ENSP00000340554.6:p.Ser25930=
|
|
ENST00000359218.10:c.77589A>G
(TTN)
|
ENSP00000352154.5:p.Ser25863=
|
|
ENST00000342175.10:c.77790A>G
(TTN)
|
ENSP00000340554.6:p.Ser25930=
|
|
ENST00000342992.10:c.96705A>G
(TTN)
|
ENSP00000343764.6:p.Ser32235=
|
|
ENST00000359218.9:c.77589A>G
(TTN)
|
ENSP00000352154.5:p.Ser25863=
|
|
ENST00000460472.6:c.77214A>G
(TTN)
|
ENSP00000434586.1:p.Ser25738=
|
|
ENST00000589042.5:c.104409A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34803=
|
|
ENST00000591111.5:c.99486A>G
(TTN)
|
ENSP00000465570.1:p.Ser33162=
|
|
ENST00000615779.4:c.99486A>G
(TTN)
|
ENSP00000483597.1:p.Ser33162=
|
|
NM_001256850.1:c.99486A>G
(TTN)
|
NP_001243779.1:p.Ser33162=
|
|
NM_001267550.2:c.104409A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34803=
|
|
NM_003319.4:c.77214A>G
(TTN)
|
NP_003310.4:p.Ser25738=
|
|
NM_133378.4:c.96705A>G
(TTN)
|
NP_596869.4:p.Ser32235=
|
|
NM_133432.3:c.77589A>G
(TTN)
|
NP_597676.3:p.Ser25863=
|
|
NM_133437.4:c.77790A>G
(TTN)
|
NP_597681.4:p.Ser25930=
|
|
NR_038271.1:n.446+8570T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3526T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103506A>G
(TTN)
|
XP_011510031.1:p.Ser34502=
|
|
XM_011511730.1:c.77400A>G
(TTN)
|
XP_011510032.1:p.Ser25800=
|
|
XM_011511731.1:c.77259A>G
(TTN)
|
XP_011510033.1:p.Ser25753=
|
|
XM_017004819.1:c.103302A>G
(TTN)
|
XP_016860308.1:p.Ser34434=
|
|
XM_017004820.1:c.98700A>G
(TTN)
|
XP_016860309.1:p.Ser32900=
|
|
XM_017004821.1:c.98697A>G
(TTN)
|
XP_016860310.1:p.Ser32899=
|
|
XM_017004822.1:c.95739A>G
(TTN)
|
XP_016860311.1:p.Ser31913=
|
|
XM_017004823.1:c.77355A>G
(TTN)
|
XP_016860312.1:p.Ser25785=
|
|
XM_024453094.1:c.98850A>G
(TTN)
|
XP_024308862.1:p.Ser32950=
|
|
XM_024453095.1:c.98847A>G
(TTN)
|
XP_024308863.1:p.Ser32949=
|
|
XM_024453096.1:c.98280A>G
(TTN)
|
XP_024308864.1:p.Ser32760=
|
|
XM_024453097.1:c.95622A>G
(TTN)
|
XP_024308865.1:p.Ser31874=
|
|
XM_024453098.1:c.95541A>G
(TTN)
|
XP_024308866.1:p.Ser31847=
|
|
XM_024453099.1:c.77304A>G
(TTN)
|
XP_024308867.1:p.Ser25768=
|
|
XM_024453100.1:c.67158A>G
(TTN)
|
XP_024308868.1:p.Ser22386=
|
|