ENST00000342992.11:c.52210T>A
(TTN)
|
ENSP00000343764.6:p.Leu17404Met
|
|
ENST00000342175.11:c.33295T>A
(TTN)
|
ENSP00000340554.6:p.Leu11099Met
|
|
ENST00000359218.10:c.33094T>A
(TTN)
|
ENSP00000352154.5:p.Leu11032Met
|
|
ENST00000342175.10:c.33295T>A
(TTN)
|
ENSP00000340554.6:p.Leu11099Met
|
|
ENST00000342992.10:c.52210T>A
(TTN)
|
ENSP00000343764.6:p.Leu17404Met
|
|
ENST00000359218.9:c.33094T>A
(TTN)
|
ENSP00000352154.5:p.Leu11032Met
|
|
ENST00000460472.6:c.32719T>A
(TTN)
|
ENSP00000434586.1:p.Leu10907Met
|
|
ENST00000589042.5:c.59914T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu19972Met
|
|
ENST00000591111.5:c.54991T>A
(TTN)
|
ENSP00000465570.1:p.Leu18331Met
|
|
ENST00000615779.4:c.54991T>A
(TTN)
|
ENSP00000483597.1:p.Leu18331Met
|
|
NM_001256850.1:c.54991T>A
(TTN)
|
NP_001243779.1:p.Leu18331Met
|
|
NM_001267550.2:c.59914T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu19972Met
|
|
NM_003319.4:c.32719T>A
(TTN)
|
NP_003310.4:p.Leu10907Met
|
|
NM_133378.4:c.52210T>A
(TTN)
|
NP_596869.4:p.Leu17404Met
|
|
NM_133432.3:c.33094T>A
(TTN)
|
NP_597676.3:p.Leu11032Met
|
|
NM_133437.4:c.33295T>A
(TTN)
|
NP_597681.4:p.Leu11099Met
|
|
NR_038271.1:n.597-5606A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+676A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.59011T>A
(TTN)
|
XP_011510031.1:p.Leu19671Met
|
|
XM_011511730.1:c.32905T>A
(TTN)
|
XP_011510032.1:p.Leu10969Met
|
|
XM_011511731.1:c.32764T>A
(TTN)
|
XP_011510033.1:p.Leu10922Met
|
|
XM_017004819.1:c.58807T>A
(TTN)
|
XP_016860308.1:p.Leu19603Met
|
|
XM_017004820.1:c.54205T>A
(TTN)
|
XP_016860309.1:p.Leu18069Met
|
|
XM_017004821.1:c.54202T>A
(TTN)
|
XP_016860310.1:p.Leu18068Met
|
|
XM_017004822.1:c.51244T>A
(TTN)
|
XP_016860311.1:p.Leu17082Met
|
|
XM_017004823.1:c.32860T>A
(TTN)
|
XP_016860312.1:p.Leu10954Met
|
|
XM_024453094.1:c.54355T>A
(TTN)
|
XP_024308862.1:p.Leu18119Met
|
|
XM_024453095.1:c.54352T>A
(TTN)
|
XP_024308863.1:p.Leu18118Met
|
|
XM_024453096.1:c.53785T>A
(TTN)
|
XP_024308864.1:p.Leu17929Met
|
|
XM_024453097.1:c.51127T>A
(TTN)
|
XP_024308865.1:p.Leu17043Met
|
|
XM_024453098.1:c.51046T>A
(TTN)
|
XP_024308866.1:p.Leu17016Met
|
|
XM_024453099.1:c.32809T>A
(TTN)
|
XP_024308867.1:p.Leu10937Met
|
|
XM_024453100.1:c.22663T>A
(TTN)
|
XP_024308868.1:p.Leu7555Met
|
|