ENST00000342992.11:c.96692C>G
(TTN)
|
ENSP00000343764.6:p.Ser32231Cys
|
|
ENST00000342175.11:c.77777C>G
(TTN)
|
ENSP00000340554.6:p.Ser25926Cys
|
|
ENST00000359218.10:c.77576C>G
(TTN)
|
ENSP00000352154.5:p.Ser25859Cys
|
|
ENST00000342175.10:c.77777C>G
(TTN)
|
ENSP00000340554.6:p.Ser25926Cys
|
|
ENST00000342992.10:c.96692C>G
(TTN)
|
ENSP00000343764.6:p.Ser32231Cys
|
|
ENST00000359218.9:c.77576C>G
(TTN)
|
ENSP00000352154.5:p.Ser25859Cys
|
|
ENST00000460472.6:c.77201C>G
(TTN)
|
ENSP00000434586.1:p.Ser25734Cys
|
|
ENST00000589042.5:c.104396C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34799Cys
|
|
ENST00000591111.5:c.99473C>G
(TTN)
|
ENSP00000465570.1:p.Ser33158Cys
|
|
ENST00000615779.4:c.99473C>G
(TTN)
|
ENSP00000483597.1:p.Ser33158Cys
|
|
NM_001256850.1:c.99473C>G
(TTN)
|
NP_001243779.1:p.Ser33158Cys
|
|
NM_001267550.2:c.104396C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34799Cys
|
|
NM_003319.4:c.77201C>G
(TTN)
|
NP_003310.4:p.Ser25734Cys
|
|
NM_133378.4:c.96692C>G
(TTN)
|
NP_596869.4:p.Ser32231Cys
|
|
NM_133432.3:c.77576C>G
(TTN)
|
NP_597676.3:p.Ser25859Cys
|
|
NM_133437.4:c.77777C>G
(TTN)
|
NP_597681.4:p.Ser25926Cys
|
|
NR_038271.1:n.446+8583G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3513G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103493C>G
(TTN)
|
XP_011510031.1:p.Ser34498Cys
|
|
XM_011511730.1:c.77387C>G
(TTN)
|
XP_011510032.1:p.Ser25796Cys
|
|
XM_011511731.1:c.77246C>G
(TTN)
|
XP_011510033.1:p.Ser25749Cys
|
|
XM_017004819.1:c.103289C>G
(TTN)
|
XP_016860308.1:p.Ser34430Cys
|
|
XM_017004820.1:c.98687C>G
(TTN)
|
XP_016860309.1:p.Ser32896Cys
|
|
XM_017004821.1:c.98684C>G
(TTN)
|
XP_016860310.1:p.Ser32895Cys
|
|
XM_017004822.1:c.95726C>G
(TTN)
|
XP_016860311.1:p.Ser31909Cys
|
|
XM_017004823.1:c.77342C>G
(TTN)
|
XP_016860312.1:p.Ser25781Cys
|
|
XM_024453094.1:c.98837C>G
(TTN)
|
XP_024308862.1:p.Ser32946Cys
|
|
XM_024453095.1:c.98834C>G
(TTN)
|
XP_024308863.1:p.Ser32945Cys
|
|
XM_024453096.1:c.98267C>G
(TTN)
|
XP_024308864.1:p.Ser32756Cys
|
|
XM_024453097.1:c.95609C>G
(TTN)
|
XP_024308865.1:p.Ser31870Cys
|
|
XM_024453098.1:c.95528C>G
(TTN)
|
XP_024308866.1:p.Ser31843Cys
|
|
XM_024453099.1:c.77291C>G
(TTN)
|
XP_024308867.1:p.Ser25764Cys
|
|
XM_024453100.1:c.67145C>G
(TTN)
|
XP_024308868.1:p.Ser22382Cys
|
|