ENST00000342992.11:c.87481T>A
(TTN)
|
ENSP00000343764.6:p.Trp29161Arg
|
|
ENST00000342175.11:c.68566T>A
(TTN)
|
ENSP00000340554.6:p.Trp22856Arg
|
|
ENST00000359218.10:c.68365T>A
(TTN)
|
ENSP00000352154.5:p.Trp22789Arg
|
|
ENST00000342175.10:c.68566T>A
(TTN)
|
ENSP00000340554.6:p.Trp22856Arg
|
|
ENST00000342992.10:c.87481T>A
(TTN)
|
ENSP00000343764.6:p.Trp29161Arg
|
|
ENST00000359218.9:c.68365T>A
(TTN)
|
ENSP00000352154.5:p.Trp22789Arg
|
|
ENST00000460472.6:c.67990T>A
(TTN)
|
ENSP00000434586.1:p.Trp22664Arg
|
|
ENST00000589042.5:c.95185T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Trp31729Arg
|
|
ENST00000591111.5:c.90262T>A
(TTN)
|
ENSP00000465570.1:p.Trp30088Arg
|
|
ENST00000615779.4:c.90262T>A
(TTN)
|
ENSP00000483597.1:p.Trp30088Arg
|
|
NM_001256850.1:c.90262T>A
(TTN)
|
NP_001243779.1:p.Trp30088Arg
|
|
NM_001267550.2:c.95185T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Trp31729Arg
|
|
NM_003319.4:c.67990T>A
(TTN)
|
NP_003310.4:p.Trp22664Arg
|
|
NM_133378.4:c.87481T>A
(TTN)
|
NP_596869.4:p.Trp29161Arg
|
|
NM_133432.3:c.68365T>A
(TTN)
|
NP_597676.3:p.Trp22789Arg
|
|
NM_133437.4:c.68566T>A
(TTN)
|
NP_597681.4:p.Trp22856Arg
|
|
NR_038271.1:n.446+22415A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+3690A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.94282T>A
(TTN)
|
XP_011510031.1:p.Trp31428Arg
|
|
XM_011511730.1:c.68176T>A
(TTN)
|
XP_011510032.1:p.Trp22726Arg
|
|
XM_011511731.1:c.68035T>A
(TTN)
|
XP_011510033.1:p.Trp22679Arg
|
|
XM_017004819.1:c.94078T>A
(TTN)
|
XP_016860308.1:p.Trp31360Arg
|
|
XM_017004820.1:c.89476T>A
(TTN)
|
XP_016860309.1:p.Trp29826Arg
|
|
XM_017004821.1:c.89473T>A
(TTN)
|
XP_016860310.1:p.Trp29825Arg
|
|
XM_017004822.1:c.86515T>A
(TTN)
|
XP_016860311.1:p.Trp28839Arg
|
|
XM_017004823.1:c.68131T>A
(TTN)
|
XP_016860312.1:p.Trp22711Arg
|
|
XM_024453094.1:c.89626T>A
(TTN)
|
XP_024308862.1:p.Trp29876Arg
|
|
XM_024453095.1:c.89623T>A
(TTN)
|
XP_024308863.1:p.Trp29875Arg
|
|
XM_024453096.1:c.89056T>A
(TTN)
|
XP_024308864.1:p.Trp29686Arg
|
|
XM_024453097.1:c.86398T>A
(TTN)
|
XP_024308865.1:p.Trp28800Arg
|
|
XM_024453098.1:c.86317T>A
(TTN)
|
XP_024308866.1:p.Trp28773Arg
|
|
XM_024453099.1:c.68080T>A
(TTN)
|
XP_024308867.1:p.Trp22694Arg
|
|
XM_024453100.1:c.57934T>A
(TTN)
|
XP_024308868.1:p.Trp19312Arg
|
|