ENST00000342992.11:c.78789G>A
(TTN)
|
ENSP00000343764.6:p.Leu26263=
|
|
ENST00000342175.11:c.59874G>A
(TTN)
|
ENSP00000340554.6:p.Leu19958=
|
|
ENST00000359218.10:c.59673G>A
(TTN)
|
ENSP00000352154.5:p.Leu19891=
|
|
ENST00000342175.10:c.59874G>A
(TTN)
|
ENSP00000340554.6:p.Leu19958=
|
|
ENST00000342992.10:c.78789G>A
(TTN)
|
ENSP00000343764.6:p.Leu26263=
|
|
ENST00000359218.9:c.59673G>A
(TTN)
|
ENSP00000352154.5:p.Leu19891=
|
|
ENST00000460472.6:c.59298G>A
(TTN)
|
ENSP00000434586.1:p.Leu19766=
|
|
ENST00000589042.5:c.86493G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu28831=
|
|
ENST00000591111.5:c.81570G>A
(TTN)
|
ENSP00000465570.1:p.Leu27190=
|
|
ENST00000615779.4:c.81570G>A
(TTN)
|
ENSP00000483597.1:p.Leu27190=
|
|
NM_001256850.1:c.81570G>A
(TTN)
|
NP_001243779.1:p.Leu27190=
|
|
NM_001267550.2:c.86493G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu28831=
|
|
NM_003319.4:c.59298G>A
(TTN)
|
NP_003310.4:p.Leu19766=
|
|
NM_133378.4:c.78789G>A
(TTN)
|
NP_596869.4:p.Leu26263=
|
|
NM_133432.3:c.59673G>A
(TTN)
|
NP_597676.3:p.Leu19891=
|
|
NM_133437.4:c.59874G>A
(TTN)
|
NP_597681.4:p.Leu19958=
|
|
NR_038271.1:n.447-11661C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17278C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.85590G>A
(TTN)
|
XP_011510031.1:p.Leu28530=
|
|
XM_011511730.1:c.59484G>A
(TTN)
|
XP_011510032.1:p.Leu19828=
|
|
XM_011511731.1:c.59343G>A
(TTN)
|
XP_011510033.1:p.Leu19781=
|
|
XM_017004819.1:c.85386G>A
(TTN)
|
XP_016860308.1:p.Leu28462=
|
|
XM_017004820.1:c.80784G>A
(TTN)
|
XP_016860309.1:p.Leu26928=
|
|
XM_017004821.1:c.80781G>A
(TTN)
|
XP_016860310.1:p.Leu26927=
|
|
XM_017004822.1:c.77823G>A
(TTN)
|
XP_016860311.1:p.Leu25941=
|
|
XM_017004823.1:c.59439G>A
(TTN)
|
XP_016860312.1:p.Leu19813=
|
|
XM_024453094.1:c.80934G>A
(TTN)
|
XP_024308862.1:p.Leu26978=
|
|
XM_024453095.1:c.80931G>A
(TTN)
|
XP_024308863.1:p.Leu26977=
|
|
XM_024453096.1:c.80364G>A
(TTN)
|
XP_024308864.1:p.Leu26788=
|
|
XM_024453097.1:c.77706G>A
(TTN)
|
XP_024308865.1:p.Leu25902=
|
|
XM_024453098.1:c.77625G>A
(TTN)
|
XP_024308866.1:p.Leu25875=
|
|
XM_024453099.1:c.59388G>A
(TTN)
|
XP_024308867.1:p.Leu19796=
|
|
XM_024453100.1:c.49242G>A
(TTN)
|
XP_024308868.1:p.Leu16414=
|
|