ENST00000342992.11:c.71232T>G
(TTN)
|
ENSP00000343764.6:p.Leu23744=
|
|
ENST00000342175.11:c.52317T>G
(TTN)
|
ENSP00000340554.6:p.Leu17439=
|
|
ENST00000359218.10:c.52116T>G
(TTN)
|
ENSP00000352154.5:p.Leu17372=
|
|
ENST00000342175.10:c.52317T>G
(TTN)
|
ENSP00000340554.6:p.Leu17439=
|
|
ENST00000342992.10:c.71232T>G
(TTN)
|
ENSP00000343764.6:p.Leu23744=
|
|
ENST00000359218.9:c.52116T>G
(TTN)
|
ENSP00000352154.5:p.Leu17372=
|
|
ENST00000460472.6:c.51741T>G
(TTN)
|
ENSP00000434586.1:p.Leu17247=
|
|
ENST00000589042.5:c.78936T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu26312=
|
|
ENST00000591111.5:c.74013T>G
(TTN)
|
ENSP00000465570.1:p.Leu24671=
|
|
ENST00000615779.4:c.74013T>G
(TTN)
|
ENSP00000483597.1:p.Leu24671=
|
|
NM_001256850.1:c.74013T>G
(TTN)
|
NP_001243779.1:p.Leu24671=
|
|
NM_001267550.2:c.78936T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu26312=
|
|
NM_003319.4:c.51741T>G
(TTN)
|
NP_003310.4:p.Leu17247=
|
|
NM_133378.4:c.71232T>G
(TTN)
|
NP_596869.4:p.Leu23744=
|
|
NM_133432.3:c.52116T>G
(TTN)
|
NP_597676.3:p.Leu17372=
|
|
NM_133437.4:c.52317T>G
(TTN)
|
NP_597681.4:p.Leu17439=
|
|
NR_038271.1:n.447-4104A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-15376A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.78033T>G
(TTN)
|
XP_011510031.1:p.Leu26011=
|
|
XM_011511730.1:c.51927T>G
(TTN)
|
XP_011510032.1:p.Leu17309=
|
|
XM_011511731.1:c.51786T>G
(TTN)
|
XP_011510033.1:p.Leu17262=
|
|
XM_017004819.1:c.77829T>G
(TTN)
|
XP_016860308.1:p.Leu25943=
|
|
XM_017004820.1:c.73227T>G
(TTN)
|
XP_016860309.1:p.Leu24409=
|
|
XM_017004821.1:c.73224T>G
(TTN)
|
XP_016860310.1:p.Leu24408=
|
|
XM_017004822.1:c.70266T>G
(TTN)
|
XP_016860311.1:p.Leu23422=
|
|
XM_017004823.1:c.51882T>G
(TTN)
|
XP_016860312.1:p.Leu17294=
|
|
XM_024453094.1:c.73377T>G
(TTN)
|
XP_024308862.1:p.Leu24459=
|
|
XM_024453095.1:c.73374T>G
(TTN)
|
XP_024308863.1:p.Leu24458=
|
|
XM_024453096.1:c.72807T>G
(TTN)
|
XP_024308864.1:p.Leu24269=
|
|
XM_024453097.1:c.70149T>G
(TTN)
|
XP_024308865.1:p.Leu23383=
|
|
XM_024453098.1:c.70068T>G
(TTN)
|
XP_024308866.1:p.Leu23356=
|
|
XM_024453099.1:c.51831T>G
(TTN)
|
XP_024308867.1:p.Leu17277=
|
|
XM_024453100.1:c.41685T>G
(TTN)
|
XP_024308868.1:p.Leu13895=
|
|