ENST00000342992.11:c.50653G>C
(TTN)
|
ENSP00000343764.6:p.Asp16885His
|
|
ENST00000342175.11:c.31738G>C
(TTN)
|
ENSP00000340554.6:p.Asp10580His
|
|
ENST00000359218.10:c.31537G>C
(TTN)
|
ENSP00000352154.5:p.Asp10513His
|
|
ENST00000342175.10:c.31738G>C
(TTN)
|
ENSP00000340554.6:p.Asp10580His
|
|
ENST00000342992.10:c.50653G>C
(TTN)
|
ENSP00000343764.6:p.Asp16885His
|
|
ENST00000359218.9:c.31537G>C
(TTN)
|
ENSP00000352154.5:p.Asp10513His
|
|
ENST00000460472.6:c.31162G>C
(TTN)
|
ENSP00000434586.1:p.Asp10388His
|
|
ENST00000589042.5:c.58357G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp19453His
|
|
ENST00000591111.5:c.53434G>C
(TTN)
|
ENSP00000465570.1:p.Asp17812His
|
|
ENST00000615779.4:c.53434G>C
(TTN)
|
ENSP00000483597.1:p.Asp17812His
|
|
NM_001256850.1:c.53434G>C
(TTN)
|
NP_001243779.1:p.Asp17812His
|
|
NM_001267550.2:c.58357G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp19453His
|
|
NM_003319.4:c.31162G>C
(TTN)
|
NP_003310.4:p.Asp10388His
|
|
NM_133378.4:c.50653G>C
(TTN)
|
NP_596869.4:p.Asp16885His
|
|
NM_133432.3:c.31537G>C
(TTN)
|
NP_597676.3:p.Asp10513His
|
|
NM_133437.4:c.31738G>C
(TTN)
|
NP_597681.4:p.Asp10580His
|
|
NR_038271.1:n.597-3560C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+2722C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.57454G>C
(TTN)
|
XP_011510031.1:p.Asp19152His
|
|
XM_011511730.1:c.31348G>C
(TTN)
|
XP_011510032.1:p.Asp10450His
|
|
XM_011511731.1:c.31207G>C
(TTN)
|
XP_011510033.1:p.Asp10403His
|
|
XM_017004819.1:c.57250G>C
(TTN)
|
XP_016860308.1:p.Asp19084His
|
|
XM_017004820.1:c.52648G>C
(TTN)
|
XP_016860309.1:p.Asp17550His
|
|
XM_017004821.1:c.52645G>C
(TTN)
|
XP_016860310.1:p.Asp17549His
|
|
XM_017004822.1:c.49687G>C
(TTN)
|
XP_016860311.1:p.Asp16563His
|
|
XM_017004823.1:c.31303G>C
(TTN)
|
XP_016860312.1:p.Asp10435His
|
|
XM_024453094.1:c.52798G>C
(TTN)
|
XP_024308862.1:p.Asp17600His
|
|
XM_024453095.1:c.52795G>C
(TTN)
|
XP_024308863.1:p.Asp17599His
|
|
XM_024453096.1:c.52228G>C
(TTN)
|
XP_024308864.1:p.Asp17410His
|
|
XM_024453097.1:c.49570G>C
(TTN)
|
XP_024308865.1:p.Asp16524His
|
|
XM_024453098.1:c.49489G>C
(TTN)
|
XP_024308866.1:p.Asp16497His
|
|
XM_024453099.1:c.31252G>C
(TTN)
|
XP_024308867.1:p.Asp10418His
|
|
XM_024453100.1:c.21106G>C
(TTN)
|
XP_024308868.1:p.Asp7036His
|
|