ENST00000342992.11:c.98502A>T
(TTN)
|
ENSP00000343764.6:p.Ser32834=
|
|
ENST00000342175.11:c.79587A>T
(TTN)
|
ENSP00000340554.6:p.Ser26529=
|
|
ENST00000359218.10:c.79386A>T
(TTN)
|
ENSP00000352154.5:p.Ser26462=
|
|
ENST00000342175.10:c.79587A>T
(TTN)
|
ENSP00000340554.6:p.Ser26529=
|
|
ENST00000342992.10:c.98502A>T
(TTN)
|
ENSP00000343764.6:p.Ser32834=
|
|
ENST00000359218.9:c.79386A>T
(TTN)
|
ENSP00000352154.5:p.Ser26462=
|
|
ENST00000460472.6:c.79011A>T
(TTN)
|
ENSP00000434586.1:p.Ser26337=
|
|
ENST00000589042.5:c.106206A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser35402=
|
|
ENST00000591111.5:c.101283A>T
(TTN)
|
ENSP00000465570.1:p.Ser33761=
|
|
ENST00000615779.4:c.101283A>T
(TTN)
|
ENSP00000483597.1:p.Ser33761=
|
|
NM_001256850.1:c.101283A>T
(TTN)
|
NP_001243779.1:p.Ser33761=
|
|
NM_001267550.2:c.106206A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ser35402=
|
|
NM_003319.4:c.79011A>T
(TTN)
|
NP_003310.4:p.Ser26337=
|
|
NM_133378.4:c.98502A>T
(TTN)
|
NP_596869.4:p.Ser32834=
|
|
NM_133432.3:c.79386A>T
(TTN)
|
NP_597676.3:p.Ser26462=
|
|
NM_133437.4:c.79587A>T
(TTN)
|
NP_597681.4:p.Ser26529=
|
|
NR_038271.1:n.446+6773T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5323T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105303A>T
(TTN)
|
XP_011510031.1:p.Ser35101=
|
|
XM_011511730.1:c.79197A>T
(TTN)
|
XP_011510032.1:p.Ser26399=
|
|
XM_011511731.1:c.79056A>T
(TTN)
|
XP_011510033.1:p.Ser26352=
|
|
XM_017004819.1:c.105099A>T
(TTN)
|
XP_016860308.1:p.Ser35033=
|
|
XM_017004820.1:c.100497A>T
(TTN)
|
XP_016860309.1:p.Ser33499=
|
|
XM_017004821.1:c.100494A>T
(TTN)
|
XP_016860310.1:p.Ser33498=
|
|
XM_017004822.1:c.97536A>T
(TTN)
|
XP_016860311.1:p.Ser32512=
|
|
XM_017004823.1:c.79152A>T
(TTN)
|
XP_016860312.1:p.Ser26384=
|
|
XM_024453094.1:c.100647A>T
(TTN)
|
XP_024308862.1:p.Ser33549=
|
|
XM_024453095.1:c.100644A>T
(TTN)
|
XP_024308863.1:p.Ser33548=
|
|
XM_024453096.1:c.100077A>T
(TTN)
|
XP_024308864.1:p.Ser33359=
|
|
XM_024453097.1:c.97419A>T
(TTN)
|
XP_024308865.1:p.Ser32473=
|
|
XM_024453098.1:c.97338A>T
(TTN)
|
XP_024308866.1:p.Ser32446=
|
|
XM_024453099.1:c.79101A>T
(TTN)
|
XP_024308867.1:p.Ser26367=
|
|
XM_024453100.1:c.68955A>T
(TTN)
|
XP_024308868.1:p.Ser22985=
|
|