ENST00000342992.11:c.51368A>G
(TTN)
|
ENSP00000343764.6:p.Asp17123Gly
|
|
ENST00000342175.11:c.32453A>G
(TTN)
|
ENSP00000340554.6:p.Asp10818Gly
|
|
ENST00000359218.10:c.32252A>G
(TTN)
|
ENSP00000352154.5:p.Asp10751Gly
|
|
ENST00000342175.10:c.32453A>G
(TTN)
|
ENSP00000340554.6:p.Asp10818Gly
|
|
ENST00000342992.10:c.51368A>G
(TTN)
|
ENSP00000343764.6:p.Asp17123Gly
|
|
ENST00000359218.9:c.32252A>G
(TTN)
|
ENSP00000352154.5:p.Asp10751Gly
|
|
ENST00000460472.6:c.31877A>G
(TTN)
|
ENSP00000434586.1:p.Asp10626Gly
|
|
ENST00000589042.5:c.59072A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp19691Gly
|
|
ENST00000591111.5:c.54149A>G
(TTN)
|
ENSP00000465570.1:p.Asp18050Gly
|
|
ENST00000615779.4:c.54149A>G
(TTN)
|
ENSP00000483597.1:p.Asp18050Gly
|
|
NM_001256850.1:c.54149A>G
(TTN)
|
NP_001243779.1:p.Asp18050Gly
|
|
NM_001267550.2:c.59072A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp19691Gly
|
|
NM_003319.4:c.31877A>G
(TTN)
|
NP_003310.4:p.Asp10626Gly
|
|
NM_133378.4:c.51368A>G
(TTN)
|
NP_596869.4:p.Asp17123Gly
|
|
NM_133432.3:c.32252A>G
(TTN)
|
NP_597676.3:p.Asp10751Gly
|
|
NM_133437.4:c.32453A>G
(TTN)
|
NP_597681.4:p.Asp10818Gly
|
|
NR_038271.1:n.597-4549T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1733T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.58169A>G
(TTN)
|
XP_011510031.1:p.Asp19390Gly
|
|
XM_011511730.1:c.32063A>G
(TTN)
|
XP_011510032.1:p.Asp10688Gly
|
|
XM_011511731.1:c.31922A>G
(TTN)
|
XP_011510033.1:p.Asp10641Gly
|
|
XM_017004819.1:c.57965A>G
(TTN)
|
XP_016860308.1:p.Asp19322Gly
|
|
XM_017004820.1:c.53363A>G
(TTN)
|
XP_016860309.1:p.Asp17788Gly
|
|
XM_017004821.1:c.53360A>G
(TTN)
|
XP_016860310.1:p.Asp17787Gly
|
|
XM_017004822.1:c.50402A>G
(TTN)
|
XP_016860311.1:p.Asp16801Gly
|
|
XM_017004823.1:c.32018A>G
(TTN)
|
XP_016860312.1:p.Asp10673Gly
|
|
XM_024453094.1:c.53513A>G
(TTN)
|
XP_024308862.1:p.Asp17838Gly
|
|
XM_024453095.1:c.53510A>G
(TTN)
|
XP_024308863.1:p.Asp17837Gly
|
|
XM_024453096.1:c.52943A>G
(TTN)
|
XP_024308864.1:p.Asp17648Gly
|
|
XM_024453097.1:c.50285A>G
(TTN)
|
XP_024308865.1:p.Asp16762Gly
|
|
XM_024453098.1:c.50204A>G
(TTN)
|
XP_024308866.1:p.Asp16735Gly
|
|
XM_024453099.1:c.31967A>G
(TTN)
|
XP_024308867.1:p.Asp10656Gly
|
|
XM_024453100.1:c.21821A>G
(TTN)
|
XP_024308868.1:p.Asp7274Gly
|
|