ENST00000342992.11:c.96691T>G
(TTN)
|
ENSP00000343764.6:p.Ser32231Ala
|
|
ENST00000342175.11:c.77776T>G
(TTN)
|
ENSP00000340554.6:p.Ser25926Ala
|
|
ENST00000359218.10:c.77575T>G
(TTN)
|
ENSP00000352154.5:p.Ser25859Ala
|
|
ENST00000342175.10:c.77776T>G
(TTN)
|
ENSP00000340554.6:p.Ser25926Ala
|
|
ENST00000342992.10:c.96691T>G
(TTN)
|
ENSP00000343764.6:p.Ser32231Ala
|
|
ENST00000359218.9:c.77575T>G
(TTN)
|
ENSP00000352154.5:p.Ser25859Ala
|
|
ENST00000460472.6:c.77200T>G
(TTN)
|
ENSP00000434586.1:p.Ser25734Ala
|
|
ENST00000589042.5:c.104395T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34799Ala
|
|
ENST00000591111.5:c.99472T>G
(TTN)
|
ENSP00000465570.1:p.Ser33158Ala
|
|
ENST00000615779.4:c.99472T>G
(TTN)
|
ENSP00000483597.1:p.Ser33158Ala
|
|
NM_001256850.1:c.99472T>G
(TTN)
|
NP_001243779.1:p.Ser33158Ala
|
|
NM_001267550.2:c.104395T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34799Ala
|
|
NM_003319.4:c.77200T>G
(TTN)
|
NP_003310.4:p.Ser25734Ala
|
|
NM_133378.4:c.96691T>G
(TTN)
|
NP_596869.4:p.Ser32231Ala
|
|
NM_133432.3:c.77575T>G
(TTN)
|
NP_597676.3:p.Ser25859Ala
|
|
NM_133437.4:c.77776T>G
(TTN)
|
NP_597681.4:p.Ser25926Ala
|
|
NR_038271.1:n.446+8584A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3512A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103492T>G
(TTN)
|
XP_011510031.1:p.Ser34498Ala
|
|
XM_011511730.1:c.77386T>G
(TTN)
|
XP_011510032.1:p.Ser25796Ala
|
|
XM_011511731.1:c.77245T>G
(TTN)
|
XP_011510033.1:p.Ser25749Ala
|
|
XM_017004819.1:c.103288T>G
(TTN)
|
XP_016860308.1:p.Ser34430Ala
|
|
XM_017004820.1:c.98686T>G
(TTN)
|
XP_016860309.1:p.Ser32896Ala
|
|
XM_017004821.1:c.98683T>G
(TTN)
|
XP_016860310.1:p.Ser32895Ala
|
|
XM_017004822.1:c.95725T>G
(TTN)
|
XP_016860311.1:p.Ser31909Ala
|
|
XM_017004823.1:c.77341T>G
(TTN)
|
XP_016860312.1:p.Ser25781Ala
|
|
XM_024453094.1:c.98836T>G
(TTN)
|
XP_024308862.1:p.Ser32946Ala
|
|
XM_024453095.1:c.98833T>G
(TTN)
|
XP_024308863.1:p.Ser32945Ala
|
|
XM_024453096.1:c.98266T>G
(TTN)
|
XP_024308864.1:p.Ser32756Ala
|
|
XM_024453097.1:c.95608T>G
(TTN)
|
XP_024308865.1:p.Ser31870Ala
|
|
XM_024453098.1:c.95527T>G
(TTN)
|
XP_024308866.1:p.Ser31843Ala
|
|
XM_024453099.1:c.77290T>G
(TTN)
|
XP_024308867.1:p.Ser25764Ala
|
|
XM_024453100.1:c.67144T>G
(TTN)
|
XP_024308868.1:p.Ser22382Ala
|
|