ENST00000342992.11:c.83762G>T
(TTN)
|
ENSP00000343764.6:p.Gly27921Val
|
|
ENST00000342175.11:c.64847G>T
(TTN)
|
ENSP00000340554.6:p.Gly21616Val
|
|
ENST00000359218.10:c.64646G>T
(TTN)
|
ENSP00000352154.5:p.Gly21549Val
|
|
ENST00000342175.10:c.64847G>T
(TTN)
|
ENSP00000340554.6:p.Gly21616Val
|
|
ENST00000342992.10:c.83762G>T
(TTN)
|
ENSP00000343764.6:p.Gly27921Val
|
|
ENST00000359218.9:c.64646G>T
(TTN)
|
ENSP00000352154.5:p.Gly21549Val
|
|
ENST00000460472.6:c.64271G>T
(TTN)
|
ENSP00000434586.1:p.Gly21424Val
|
|
ENST00000589042.5:c.91466G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly30489Val
|
|
ENST00000591111.5:c.86543G>T
(TTN)
|
ENSP00000465570.1:p.Gly28848Val
|
|
ENST00000615779.4:c.86543G>T
(TTN)
|
ENSP00000483597.1:p.Gly28848Val
|
|
NM_001256850.1:c.86543G>T
(TTN)
|
NP_001243779.1:p.Gly28848Val
|
|
NM_001267550.2:c.91466G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly30489Val
|
|
NM_003319.4:c.64271G>T
(TTN)
|
NP_003310.4:p.Gly21424Val
|
|
NM_133378.4:c.83762G>T
(TTN)
|
NP_596869.4:p.Gly27921Val
|
|
NM_133432.3:c.64646G>T
(TTN)
|
NP_597676.3:p.Gly21549Val
|
|
NM_133437.4:c.64847G>T
(TTN)
|
NP_597681.4:p.Gly21616Val
|
|
NR_038271.1:n.447-20235C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+8704C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.90563G>T
(TTN)
|
XP_011510031.1:p.Gly30188Val
|
|
XM_011511730.1:c.64457G>T
(TTN)
|
XP_011510032.1:p.Gly21486Val
|
|
XM_011511731.1:c.64316G>T
(TTN)
|
XP_011510033.1:p.Gly21439Val
|
|
XM_017004819.1:c.90359G>T
(TTN)
|
XP_016860308.1:p.Gly30120Val
|
|
XM_017004820.1:c.85757G>T
(TTN)
|
XP_016860309.1:p.Gly28586Val
|
|
XM_017004821.1:c.85754G>T
(TTN)
|
XP_016860310.1:p.Gly28585Val
|
|
XM_017004822.1:c.82796G>T
(TTN)
|
XP_016860311.1:p.Gly27599Val
|
|
XM_017004823.1:c.64412G>T
(TTN)
|
XP_016860312.1:p.Gly21471Val
|
|
XM_024453094.1:c.85907G>T
(TTN)
|
XP_024308862.1:p.Gly28636Val
|
|
XM_024453095.1:c.85904G>T
(TTN)
|
XP_024308863.1:p.Gly28635Val
|
|
XM_024453096.1:c.85337G>T
(TTN)
|
XP_024308864.1:p.Gly28446Val
|
|
XM_024453097.1:c.82679G>T
(TTN)
|
XP_024308865.1:p.Gly27560Val
|
|
XM_024453098.1:c.82598G>T
(TTN)
|
XP_024308866.1:p.Gly27533Val
|
|
XM_024453099.1:c.64361G>T
(TTN)
|
XP_024308867.1:p.Gly21454Val
|
|
XM_024453100.1:c.54215G>T
(TTN)
|
XP_024308868.1:p.Gly18072Val
|
|