ENST00000342992.11:c.41642A>G
(TTN)
|
ENSP00000343764.6:p.Asp13881Gly
|
|
ENST00000342175.11:c.22727A>G
(TTN)
|
ENSP00000340554.6:p.Asp7576Gly
|
|
ENST00000359218.10:c.22526A>G
(TTN)
|
ENSP00000352154.5:p.Asp7509Gly
|
|
ENST00000342175.10:c.22727A>G
(TTN)
|
ENSP00000340554.6:p.Asp7576Gly
|
|
ENST00000342992.10:c.41642A>G
(TTN)
|
ENSP00000343764.6:p.Asp13881Gly
|
|
ENST00000359218.9:c.22526A>G
(TTN)
|
ENSP00000352154.5:p.Asp7509Gly
|
|
ENST00000460472.6:c.22151A>G
(TTN)
|
ENSP00000434586.1:p.Asp7384Gly
|
|
ENST00000589042.5:c.49346A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp16449Gly
|
|
ENST00000591111.5:c.44423A>G
(TTN)
|
ENSP00000465570.1:p.Asp14808Gly
|
|
ENST00000615779.4:c.44423A>G
(TTN)
|
ENSP00000483597.1:p.Asp14808Gly
|
|
NM_001256850.1:c.44423A>G
(TTN)
|
NP_001243779.1:p.Asp14808Gly
|
|
NM_001267550.2:c.49346A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp16449Gly
|
|
NM_003319.4:c.22151A>G
(TTN)
|
NP_003310.4:p.Asp7384Gly
|
|
NM_133378.4:c.41642A>G
(TTN)
|
NP_596869.4:p.Asp13881Gly
|
|
NM_133432.3:c.22526A>G
(TTN)
|
NP_597676.3:p.Asp7509Gly
|
|
NM_133437.4:c.22727A>G
(TTN)
|
NP_597681.4:p.Asp7576Gly
|
|
NR_038271.1:n.783-98T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.48443A>G
(TTN)
|
XP_011510031.1:p.Asp16148Gly
|
|
XM_011511730.1:c.22337A>G
(TTN)
|
XP_011510032.1:p.Asp7446Gly
|
|
XM_011511731.1:c.22196A>G
(TTN)
|
XP_011510033.1:p.Asp7399Gly
|
|
XM_017004819.1:c.48239A>G
(TTN)
|
XP_016860308.1:p.Asp16080Gly
|
|
XM_017004820.1:c.43637A>G
(TTN)
|
XP_016860309.1:p.Asp14546Gly
|
|
XM_017004821.1:c.43634A>G
(TTN)
|
XP_016860310.1:p.Asp14545Gly
|
|
XM_017004822.1:c.40676A>G
(TTN)
|
XP_016860311.1:p.Asp13559Gly
|
|
XM_017004823.1:c.22292A>G
(TTN)
|
XP_016860312.1:p.Asp7431Gly
|
|
XM_024453094.1:c.43787A>G
(TTN)
|
XP_024308862.1:p.Asp14596Gly
|
|
XM_024453095.1:c.43784A>G
(TTN)
|
XP_024308863.1:p.Asp14595Gly
|
|
XM_024453096.1:c.43217A>G
(TTN)
|
XP_024308864.1:p.Asp14406Gly
|
|
XM_024453097.1:c.40559A>G
(TTN)
|
XP_024308865.1:p.Asp13520Gly
|
|
XM_024453098.1:c.40478A>G
(TTN)
|
XP_024308866.1:p.Asp13493Gly
|
|
XM_024453099.1:c.22241A>G
(TTN)
|
XP_024308867.1:p.Asp7414Gly
|
|
XM_024453100.1:c.12095A>G
(TTN)
|
XP_024308868.1:p.Asp4032Gly
|
|