ENST00000342992.11:c.96704C>A
(TTN)
|
ENSP00000343764.6:p.Ser32235Ter
|
|
ENST00000342175.11:c.77789C>A
(TTN)
|
ENSP00000340554.6:p.Ser25930Ter
|
|
ENST00000359218.10:c.77588C>A
(TTN)
|
ENSP00000352154.5:p.Ser25863Ter
|
|
ENST00000342175.10:c.77789C>A
(TTN)
|
ENSP00000340554.6:p.Ser25930Ter
|
|
ENST00000342992.10:c.96704C>A
(TTN)
|
ENSP00000343764.6:p.Ser32235Ter
|
|
ENST00000359218.9:c.77588C>A
(TTN)
|
ENSP00000352154.5:p.Ser25863Ter
|
|
ENST00000460472.6:c.77213C>A
(TTN)
|
ENSP00000434586.1:p.Ser25738Ter
|
|
ENST00000589042.5:c.104408C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34803Ter
|
|
ENST00000591111.5:c.99485C>A
(TTN)
|
ENSP00000465570.1:p.Ser33162Ter
|
|
ENST00000615779.4:c.99485C>A
(TTN)
|
ENSP00000483597.1:p.Ser33162Ter
|
|
NM_001256850.1:c.99485C>A
(TTN)
|
NP_001243779.1:p.Ser33162Ter
|
|
NM_001267550.2:c.104408C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34803Ter
|
|
NM_003319.4:c.77213C>A
(TTN)
|
NP_003310.4:p.Ser25738Ter
|
|
NM_133378.4:c.96704C>A
(TTN)
|
NP_596869.4:p.Ser32235Ter
|
|
NM_133432.3:c.77588C>A
(TTN)
|
NP_597676.3:p.Ser25863Ter
|
|
NM_133437.4:c.77789C>A
(TTN)
|
NP_597681.4:p.Ser25930Ter
|
|
NR_038271.1:n.446+8571G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3525G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103505C>A
(TTN)
|
XP_011510031.1:p.Ser34502Ter
|
|
XM_011511730.1:c.77399C>A
(TTN)
|
XP_011510032.1:p.Ser25800Ter
|
|
XM_011511731.1:c.77258C>A
(TTN)
|
XP_011510033.1:p.Ser25753Ter
|
|
XM_017004819.1:c.103301C>A
(TTN)
|
XP_016860308.1:p.Ser34434Ter
|
|
XM_017004820.1:c.98699C>A
(TTN)
|
XP_016860309.1:p.Ser32900Ter
|
|
XM_017004821.1:c.98696C>A
(TTN)
|
XP_016860310.1:p.Ser32899Ter
|
|
XM_017004822.1:c.95738C>A
(TTN)
|
XP_016860311.1:p.Ser31913Ter
|
|
XM_017004823.1:c.77354C>A
(TTN)
|
XP_016860312.1:p.Ser25785Ter
|
|
XM_024453094.1:c.98849C>A
(TTN)
|
XP_024308862.1:p.Ser32950Ter
|
|
XM_024453095.1:c.98846C>A
(TTN)
|
XP_024308863.1:p.Ser32949Ter
|
|
XM_024453096.1:c.98279C>A
(TTN)
|
XP_024308864.1:p.Ser32760Ter
|
|
XM_024453097.1:c.95621C>A
(TTN)
|
XP_024308865.1:p.Ser31874Ter
|
|
XM_024453098.1:c.95540C>A
(TTN)
|
XP_024308866.1:p.Ser31847Ter
|
|
XM_024453099.1:c.77303C>A
(TTN)
|
XP_024308867.1:p.Ser25768Ter
|
|
XM_024453100.1:c.67157C>A
(TTN)
|
XP_024308868.1:p.Ser22386Ter
|
|