ENST00000342992.11:c.98703T>A
(TTN)
|
ENSP00000343764.6:p.Ser32901=
|
|
ENST00000342175.11:c.79788T>A
(TTN)
|
ENSP00000340554.6:p.Ser26596=
|
|
ENST00000359218.10:c.79587T>A
(TTN)
|
ENSP00000352154.5:p.Ser26529=
|
|
ENST00000342175.10:c.79788T>A
(TTN)
|
ENSP00000340554.6:p.Ser26596=
|
|
ENST00000342992.10:c.98703T>A
(TTN)
|
ENSP00000343764.6:p.Ser32901=
|
|
ENST00000359218.9:c.79587T>A
(TTN)
|
ENSP00000352154.5:p.Ser26529=
|
|
ENST00000460472.6:c.79212T>A
(TTN)
|
ENSP00000434586.1:p.Ser26404=
|
|
ENST00000589042.5:c.106407T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser35469=
|
|
ENST00000591111.5:c.101484T>A
(TTN)
|
ENSP00000465570.1:p.Ser33828=
|
|
ENST00000615779.4:c.101484T>A
(TTN)
|
ENSP00000483597.1:p.Ser33828=
|
|
NM_001256850.1:c.101484T>A
(TTN)
|
NP_001243779.1:p.Ser33828=
|
|
NM_001267550.2:c.106407T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser35469=
|
|
NM_003319.4:c.79212T>A
(TTN)
|
NP_003310.4:p.Ser26404=
|
|
NM_133378.4:c.98703T>A
(TTN)
|
NP_596869.4:p.Ser32901=
|
|
NM_133432.3:c.79587T>A
(TTN)
|
NP_597676.3:p.Ser26529=
|
|
NM_133437.4:c.79788T>A
(TTN)
|
NP_597681.4:p.Ser26596=
|
|
NR_038271.1:n.446+6448A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5648A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105504T>A
(TTN)
|
XP_011510031.1:p.Ser35168=
|
|
XM_011511730.1:c.79398T>A
(TTN)
|
XP_011510032.1:p.Ser26466=
|
|
XM_011511731.1:c.79257T>A
(TTN)
|
XP_011510033.1:p.Ser26419=
|
|
XM_017004819.1:c.105300T>A
(TTN)
|
XP_016860308.1:p.Ser35100=
|
|
XM_017004820.1:c.100698T>A
(TTN)
|
XP_016860309.1:p.Ser33566=
|
|
XM_017004821.1:c.100695T>A
(TTN)
|
XP_016860310.1:p.Ser33565=
|
|
XM_017004822.1:c.97737T>A
(TTN)
|
XP_016860311.1:p.Ser32579=
|
|
XM_017004823.1:c.79353T>A
(TTN)
|
XP_016860312.1:p.Ser26451=
|
|
XM_024453094.1:c.100848T>A
(TTN)
|
XP_024308862.1:p.Ser33616=
|
|
XM_024453095.1:c.100845T>A
(TTN)
|
XP_024308863.1:p.Ser33615=
|
|
XM_024453096.1:c.100278T>A
(TTN)
|
XP_024308864.1:p.Ser33426=
|
|
XM_024453097.1:c.97620T>A
(TTN)
|
XP_024308865.1:p.Ser32540=
|
|
XM_024453098.1:c.97539T>A
(TTN)
|
XP_024308866.1:p.Ser32513=
|
|
XM_024453099.1:c.79302T>A
(TTN)
|
XP_024308867.1:p.Ser26434=
|
|
XM_024453100.1:c.69156T>A
(TTN)
|
XP_024308868.1:p.Ser23052=
|
|