ENST00000342992.11:c.47360C>A
(TTN)
|
ENSP00000343764.6:p.Ala15787Asp
|
|
ENST00000342175.11:c.28445C>A
(TTN)
|
ENSP00000340554.6:p.Ala9482Asp
|
|
ENST00000359218.10:c.28244C>A
(TTN)
|
ENSP00000352154.5:p.Ala9415Asp
|
|
ENST00000342175.10:c.28445C>A
(TTN)
|
ENSP00000340554.6:p.Ala9482Asp
|
|
ENST00000342992.10:c.47360C>A
(TTN)
|
ENSP00000343764.6:p.Ala15787Asp
|
|
ENST00000359218.9:c.28244C>A
(TTN)
|
ENSP00000352154.5:p.Ala9415Asp
|
|
ENST00000460472.6:c.27869C>A
(TTN)
|
ENSP00000434586.1:p.Ala9290Asp
|
|
ENST00000589042.5:c.55064C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala18355Asp
|
|
ENST00000591111.5:c.50141C>A
(TTN)
|
ENSP00000465570.1:p.Ala16714Asp
|
|
ENST00000615779.4:c.50141C>A
(TTN)
|
ENSP00000483597.1:p.Ala16714Asp
|
|
NM_001256850.1:c.50141C>A
(TTN)
|
NP_001243779.1:p.Ala16714Asp
|
|
NM_001267550.2:c.55064C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala18355Asp
|
|
NM_003319.4:c.27869C>A
(TTN)
|
NP_003310.4:p.Ala9290Asp
|
|
NM_133378.4:c.47360C>A
(TTN)
|
NP_596869.4:p.Ala15787Asp
|
|
NM_133432.3:c.28244C>A
(TTN)
|
NP_597676.3:p.Ala9415Asp
|
|
NM_133437.4:c.28445C>A
(TTN)
|
NP_597681.4:p.Ala9482Asp
|
|
NR_038271.1:n.682+4657G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+1671G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.54161C>A
(TTN)
|
XP_011510031.1:p.Ala18054Asp
|
|
XM_011511730.1:c.28055C>A
(TTN)
|
XP_011510032.1:p.Ala9352Asp
|
|
XM_011511731.1:c.27914C>A
(TTN)
|
XP_011510033.1:p.Ala9305Asp
|
|
XM_017004819.1:c.53957C>A
(TTN)
|
XP_016860308.1:p.Ala17986Asp
|
|
XM_017004820.1:c.49355C>A
(TTN)
|
XP_016860309.1:p.Ala16452Asp
|
|
XM_017004821.1:c.49352C>A
(TTN)
|
XP_016860310.1:p.Ala16451Asp
|
|
XM_017004822.1:c.46394C>A
(TTN)
|
XP_016860311.1:p.Ala15465Asp
|
|
XM_017004823.1:c.28010C>A
(TTN)
|
XP_016860312.1:p.Ala9337Asp
|
|
XM_024453094.1:c.49505C>A
(TTN)
|
XP_024308862.1:p.Ala16502Asp
|
|
XM_024453095.1:c.49502C>A
(TTN)
|
XP_024308863.1:p.Ala16501Asp
|
|
XM_024453096.1:c.48935C>A
(TTN)
|
XP_024308864.1:p.Ala16312Asp
|
|
XM_024453097.1:c.46277C>A
(TTN)
|
XP_024308865.1:p.Ala15426Asp
|
|
XM_024453098.1:c.46196C>A
(TTN)
|
XP_024308866.1:p.Ala15399Asp
|
|
XM_024453099.1:c.27959C>A
(TTN)
|
XP_024308867.1:p.Ala9320Asp
|
|
XM_024453100.1:c.17813C>A
(TTN)
|
XP_024308868.1:p.Ala5938Asp
|
|