ENST00000342992.11:c.98468A>T
(TTN)
|
ENSP00000343764.6:p.Glu32823Val
|
|
ENST00000342175.11:c.79553A>T
(TTN)
|
ENSP00000340554.6:p.Glu26518Val
|
|
ENST00000359218.10:c.79352A>T
(TTN)
|
ENSP00000352154.5:p.Glu26451Val
|
|
ENST00000342175.10:c.79553A>T
(TTN)
|
ENSP00000340554.6:p.Glu26518Val
|
|
ENST00000342992.10:c.98468A>T
(TTN)
|
ENSP00000343764.6:p.Glu32823Val
|
|
ENST00000359218.9:c.79352A>T
(TTN)
|
ENSP00000352154.5:p.Glu26451Val
|
|
ENST00000460472.6:c.78977A>T
(TTN)
|
ENSP00000434586.1:p.Glu26326Val
|
|
ENST00000589042.5:c.106172A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35391Val
|
|
ENST00000591111.5:c.101249A>T
(TTN)
|
ENSP00000465570.1:p.Glu33750Val
|
|
ENST00000615779.4:c.101249A>T
(TTN)
|
ENSP00000483597.1:p.Glu33750Val
|
|
NM_001256850.1:c.101249A>T
(TTN)
|
NP_001243779.1:p.Glu33750Val
|
|
NM_001267550.2:c.106172A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35391Val
|
|
NM_003319.4:c.78977A>T
(TTN)
|
NP_003310.4:p.Glu26326Val
|
|
NM_133378.4:c.98468A>T
(TTN)
|
NP_596869.4:p.Glu32823Val
|
|
NM_133432.3:c.79352A>T
(TTN)
|
NP_597676.3:p.Glu26451Val
|
|
NM_133437.4:c.79553A>T
(TTN)
|
NP_597681.4:p.Glu26518Val
|
|
NR_038271.1:n.446+6807T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5289T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105269A>T
(TTN)
|
XP_011510031.1:p.Glu35090Val
|
|
XM_011511730.1:c.79163A>T
(TTN)
|
XP_011510032.1:p.Glu26388Val
|
|
XM_011511731.1:c.79022A>T
(TTN)
|
XP_011510033.1:p.Glu26341Val
|
|
XM_017004819.1:c.105065A>T
(TTN)
|
XP_016860308.1:p.Glu35022Val
|
|
XM_017004820.1:c.100463A>T
(TTN)
|
XP_016860309.1:p.Glu33488Val
|
|
XM_017004821.1:c.100460A>T
(TTN)
|
XP_016860310.1:p.Glu33487Val
|
|
XM_017004822.1:c.97502A>T
(TTN)
|
XP_016860311.1:p.Glu32501Val
|
|
XM_017004823.1:c.79118A>T
(TTN)
|
XP_016860312.1:p.Glu26373Val
|
|
XM_024453094.1:c.100613A>T
(TTN)
|
XP_024308862.1:p.Glu33538Val
|
|
XM_024453095.1:c.100610A>T
(TTN)
|
XP_024308863.1:p.Glu33537Val
|
|
XM_024453096.1:c.100043A>T
(TTN)
|
XP_024308864.1:p.Glu33348Val
|
|
XM_024453097.1:c.97385A>T
(TTN)
|
XP_024308865.1:p.Glu32462Val
|
|
XM_024453098.1:c.97304A>T
(TTN)
|
XP_024308866.1:p.Glu32435Val
|
|
XM_024453099.1:c.79067A>T
(TTN)
|
XP_024308867.1:p.Glu26356Val
|
|
XM_024453100.1:c.68921A>T
(TTN)
|
XP_024308868.1:p.Glu22974Val
|
|