ENST00000342992.11:c.83364T>G
(TTN)
|
ENSP00000343764.6:p.Val27788=
|
|
ENST00000342175.11:c.64449T>G
(TTN)
|
ENSP00000340554.6:p.Val21483=
|
|
ENST00000359218.10:c.64248T>G
(TTN)
|
ENSP00000352154.5:p.Val21416=
|
|
ENST00000342175.10:c.64449T>G
(TTN)
|
ENSP00000340554.6:p.Val21483=
|
|
ENST00000342992.10:c.83364T>G
(TTN)
|
ENSP00000343764.6:p.Val27788=
|
|
ENST00000359218.9:c.64248T>G
(TTN)
|
ENSP00000352154.5:p.Val21416=
|
|
ENST00000460472.6:c.63873T>G
(TTN)
|
ENSP00000434586.1:p.Val21291=
|
|
ENST00000589042.5:c.91068T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val30356=
|
|
ENST00000591111.5:c.86145T>G
(TTN)
|
ENSP00000465570.1:p.Val28715=
|
|
ENST00000615779.4:c.86145T>G
(TTN)
|
ENSP00000483597.1:p.Val28715=
|
|
NM_001256850.1:c.86145T>G
(TTN)
|
NP_001243779.1:p.Val28715=
|
|
NM_001267550.2:c.91068T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val30356=
|
|
NM_003319.4:c.63873T>G
(TTN)
|
NP_003310.4:p.Val21291=
|
|
NM_133378.4:c.83364T>G
(TTN)
|
NP_596869.4:p.Val27788=
|
|
NM_133432.3:c.64248T>G
(TTN)
|
NP_597676.3:p.Val21416=
|
|
NM_133437.4:c.64449T>G
(TTN)
|
NP_597681.4:p.Val21483=
|
|
NR_038271.1:n.447-19468A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9471A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.90165T>G
(TTN)
|
XP_011510031.1:p.Val30055=
|
|
XM_011511730.1:c.64059T>G
(TTN)
|
XP_011510032.1:p.Val21353=
|
|
XM_011511731.1:c.63918T>G
(TTN)
|
XP_011510033.1:p.Val21306=
|
|
XM_017004819.1:c.89961T>G
(TTN)
|
XP_016860308.1:p.Val29987=
|
|
XM_017004820.1:c.85359T>G
(TTN)
|
XP_016860309.1:p.Val28453=
|
|
XM_017004821.1:c.85356T>G
(TTN)
|
XP_016860310.1:p.Val28452=
|
|
XM_017004822.1:c.82398T>G
(TTN)
|
XP_016860311.1:p.Val27466=
|
|
XM_017004823.1:c.64014T>G
(TTN)
|
XP_016860312.1:p.Val21338=
|
|
XM_024453094.1:c.85509T>G
(TTN)
|
XP_024308862.1:p.Val28503=
|
|
XM_024453095.1:c.85506T>G
(TTN)
|
XP_024308863.1:p.Val28502=
|
|
XM_024453096.1:c.84939T>G
(TTN)
|
XP_024308864.1:p.Val28313=
|
|
XM_024453097.1:c.82281T>G
(TTN)
|
XP_024308865.1:p.Val27427=
|
|
XM_024453098.1:c.82200T>G
(TTN)
|
XP_024308866.1:p.Val27400=
|
|
XM_024453099.1:c.63963T>G
(TTN)
|
XP_024308867.1:p.Val21321=
|
|
XM_024453100.1:c.53817T>G
(TTN)
|
XP_024308868.1:p.Val17939=
|
|