ENST00000342992.11:c.88343T>G
(TTN)
|
ENSP00000343764.6:p.Leu29448Arg
|
|
ENST00000342175.11:c.69428T>G
(TTN)
|
ENSP00000340554.6:p.Leu23143Arg
|
|
ENST00000359218.10:c.69227T>G
(TTN)
|
ENSP00000352154.5:p.Leu23076Arg
|
|
ENST00000342175.10:c.69428T>G
(TTN)
|
ENSP00000340554.6:p.Leu23143Arg
|
|
ENST00000342992.10:c.88343T>G
(TTN)
|
ENSP00000343764.6:p.Leu29448Arg
|
|
ENST00000359218.9:c.69227T>G
(TTN)
|
ENSP00000352154.5:p.Leu23076Arg
|
|
ENST00000460472.6:c.68852T>G
(TTN)
|
ENSP00000434586.1:p.Leu22951Arg
|
|
ENST00000589042.5:c.96047T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu32016Arg
|
|
ENST00000591111.5:c.91124T>G
(TTN)
|
ENSP00000465570.1:p.Leu30375Arg
|
|
ENST00000615779.4:c.91124T>G
(TTN)
|
ENSP00000483597.1:p.Leu30375Arg
|
|
NM_001256850.1:c.91124T>G
(TTN)
|
NP_001243779.1:p.Leu30375Arg
|
|
NM_001267550.2:c.96047T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu32016Arg
|
|
NM_003319.4:c.68852T>G
(TTN)
|
NP_003310.4:p.Leu22951Arg
|
|
NM_133378.4:c.88343T>G
(TTN)
|
NP_596869.4:p.Leu29448Arg
|
|
NM_133432.3:c.69227T>G
(TTN)
|
NP_597676.3:p.Leu23076Arg
|
|
NM_133437.4:c.69428T>G
(TTN)
|
NP_597681.4:p.Leu23143Arg
|
|
NR_038271.1:n.446+20461A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1736A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.95144T>G
(TTN)
|
XP_011510031.1:p.Leu31715Arg
|
|
XM_011511730.1:c.69038T>G
(TTN)
|
XP_011510032.1:p.Leu23013Arg
|
|
XM_011511731.1:c.68897T>G
(TTN)
|
XP_011510033.1:p.Leu22966Arg
|
|
XM_017004819.1:c.94940T>G
(TTN)
|
XP_016860308.1:p.Leu31647Arg
|
|
XM_017004820.1:c.90338T>G
(TTN)
|
XP_016860309.1:p.Leu30113Arg
|
|
XM_017004821.1:c.90335T>G
(TTN)
|
XP_016860310.1:p.Leu30112Arg
|
|
XM_017004822.1:c.87377T>G
(TTN)
|
XP_016860311.1:p.Leu29126Arg
|
|
XM_017004823.1:c.68993T>G
(TTN)
|
XP_016860312.1:p.Leu22998Arg
|
|
XM_024453094.1:c.90488T>G
(TTN)
|
XP_024308862.1:p.Leu30163Arg
|
|
XM_024453095.1:c.90485T>G
(TTN)
|
XP_024308863.1:p.Leu30162Arg
|
|
XM_024453096.1:c.89918T>G
(TTN)
|
XP_024308864.1:p.Leu29973Arg
|
|
XM_024453097.1:c.87260T>G
(TTN)
|
XP_024308865.1:p.Leu29087Arg
|
|
XM_024453098.1:c.87179T>G
(TTN)
|
XP_024308866.1:p.Leu29060Arg
|
|
XM_024453099.1:c.68942T>G
(TTN)
|
XP_024308867.1:p.Leu22981Arg
|
|
XM_024453100.1:c.58796T>G
(TTN)
|
XP_024308868.1:p.Leu19599Arg
|
|