ENST00000342992.11:c.39558T>C
(TTN)
|
ENSP00000343764.6:p.Ser13186=
|
|
ENST00000342175.11:c.20643T>C
(TTN)
|
ENSP00000340554.6:p.Ser6881=
|
|
ENST00000359218.10:c.20442T>C
(TTN)
|
ENSP00000352154.5:p.Ser6814=
|
|
ENST00000342175.10:c.20643T>C
(TTN)
|
ENSP00000340554.6:p.Ser6881=
|
|
ENST00000342992.10:c.39558T>C
(TTN)
|
ENSP00000343764.6:p.Ser13186=
|
|
ENST00000359218.9:c.20442T>C
(TTN)
|
ENSP00000352154.5:p.Ser6814=
|
|
ENST00000460472.6:c.20067T>C
(TTN)
|
ENSP00000434586.1:p.Ser6689=
|
|
ENST00000589042.5:c.47262T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser15754=
|
|
ENST00000591111.5:c.42339T>C
(TTN)
|
ENSP00000465570.1:p.Ser14113=
|
|
ENST00000615779.4:c.42339T>C
(TTN)
|
ENSP00000483597.1:p.Ser14113=
|
|
NM_001256850.1:c.42339T>C
(TTN)
|
NP_001243779.1:p.Ser14113=
|
|
NM_001267550.2:c.47262T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ser15754=
|
|
NM_003319.4:c.20067T>C
(TTN)
|
NP_003310.4:p.Ser6689=
|
|
NM_133378.4:c.39558T>C
(TTN)
|
NP_596869.4:p.Ser13186=
|
|
NM_133432.3:c.20442T>C
(TTN)
|
NP_597676.3:p.Ser6814=
|
|
NM_133437.4:c.20643T>C
(TTN)
|
NP_597681.4:p.Ser6881=
|
|
NR_038271.1:n.1605-1557A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.46359T>C
(TTN)
|
XP_011510031.1:p.Ser15453=
|
|
XM_011511730.1:c.20253T>C
(TTN)
|
XP_011510032.1:p.Ser6751=
|
|
XM_011511731.1:c.20112T>C
(TTN)
|
XP_011510033.1:p.Ser6704=
|
|
XM_017004819.1:c.46155T>C
(TTN)
|
XP_016860308.1:p.Ser15385=
|
|
XM_017004820.1:c.41553T>C
(TTN)
|
XP_016860309.1:p.Ser13851=
|
|
XM_017004821.1:c.41550T>C
(TTN)
|
XP_016860310.1:p.Ser13850=
|
|
XM_017004822.1:c.38592T>C
(TTN)
|
XP_016860311.1:p.Ser12864=
|
|
XM_017004823.1:c.20208T>C
(TTN)
|
XP_016860312.1:p.Ser6736=
|
|
XM_024453094.1:c.41703T>C
(TTN)
|
XP_024308862.1:p.Ser13901=
|
|
XM_024453095.1:c.41700T>C
(TTN)
|
XP_024308863.1:p.Ser13900=
|
|
XM_024453096.1:c.41133T>C
(TTN)
|
XP_024308864.1:p.Ser13711=
|
|
XM_024453097.1:c.38475T>C
(TTN)
|
XP_024308865.1:p.Ser12825=
|
|
XM_024453098.1:c.38394T>C
(TTN)
|
XP_024308866.1:p.Ser12798=
|
|
XM_024453099.1:c.20157T>C
(TTN)
|
XP_024308867.1:p.Ser6719=
|
|
XM_024453100.1:c.10011T>C
(TTN)
|
XP_024308868.1:p.Ser3337=
|
|