ENST00000342992.11:c.98428G>T
(TTN)
|
ENSP00000343764.6:p.Ala32810Ser
|
|
ENST00000342175.11:c.79513G>T
(TTN)
|
ENSP00000340554.6:p.Ala26505Ser
|
|
ENST00000359218.10:c.79312G>T
(TTN)
|
ENSP00000352154.5:p.Ala26438Ser
|
|
ENST00000342175.10:c.79513G>T
(TTN)
|
ENSP00000340554.6:p.Ala26505Ser
|
|
ENST00000342992.10:c.98428G>T
(TTN)
|
ENSP00000343764.6:p.Ala32810Ser
|
|
ENST00000359218.9:c.79312G>T
(TTN)
|
ENSP00000352154.5:p.Ala26438Ser
|
|
ENST00000460472.6:c.78937G>T
(TTN)
|
ENSP00000434586.1:p.Ala26313Ser
|
|
ENST00000589042.5:c.106132G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala35378Ser
|
|
ENST00000591111.5:c.101209G>T
(TTN)
|
ENSP00000465570.1:p.Ala33737Ser
|
|
ENST00000615779.4:c.101209G>T
(TTN)
|
ENSP00000483597.1:p.Ala33737Ser
|
|
NM_001256850.1:c.101209G>T
(TTN)
|
NP_001243779.1:p.Ala33737Ser
|
|
NM_001267550.2:c.106132G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala35378Ser
|
|
NM_003319.4:c.78937G>T
(TTN)
|
NP_003310.4:p.Ala26313Ser
|
|
NM_133378.4:c.98428G>T
(TTN)
|
NP_596869.4:p.Ala32810Ser
|
|
NM_133432.3:c.79312G>T
(TTN)
|
NP_597676.3:p.Ala26438Ser
|
|
NM_133437.4:c.79513G>T
(TTN)
|
NP_597681.4:p.Ala26505Ser
|
|
NR_038271.1:n.446+6847C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5249C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105229G>T
(TTN)
|
XP_011510031.1:p.Ala35077Ser
|
|
XM_011511730.1:c.79123G>T
(TTN)
|
XP_011510032.1:p.Ala26375Ser
|
|
XM_011511731.1:c.78982G>T
(TTN)
|
XP_011510033.1:p.Ala26328Ser
|
|
XM_017004819.1:c.105025G>T
(TTN)
|
XP_016860308.1:p.Ala35009Ser
|
|
XM_017004820.1:c.100423G>T
(TTN)
|
XP_016860309.1:p.Ala33475Ser
|
|
XM_017004821.1:c.100420G>T
(TTN)
|
XP_016860310.1:p.Ala33474Ser
|
|
XM_017004822.1:c.97462G>T
(TTN)
|
XP_016860311.1:p.Ala32488Ser
|
|
XM_017004823.1:c.79078G>T
(TTN)
|
XP_016860312.1:p.Ala26360Ser
|
|
XM_024453094.1:c.100573G>T
(TTN)
|
XP_024308862.1:p.Ala33525Ser
|
|
XM_024453095.1:c.100570G>T
(TTN)
|
XP_024308863.1:p.Ala33524Ser
|
|
XM_024453096.1:c.100003G>T
(TTN)
|
XP_024308864.1:p.Ala33335Ser
|
|
XM_024453097.1:c.97345G>T
(TTN)
|
XP_024308865.1:p.Ala32449Ser
|
|
XM_024453098.1:c.97264G>T
(TTN)
|
XP_024308866.1:p.Ala32422Ser
|
|
XM_024453099.1:c.79027G>T
(TTN)
|
XP_024308867.1:p.Ala26343Ser
|
|
XM_024453100.1:c.68881G>T
(TTN)
|
XP_024308868.1:p.Ala22961Ser
|
|