|
NM_001267550.2:c.54717C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly18239=
|
|
ENST00000589042.5:c.54717C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly18239=
|
|
NM_001256850.1:c.49794C>T
(TTN)
|
NP_001243779.1:p.Gly16598=
|
|
NM_003319.4:c.27522C>T
(TTN)
|
NP_003310.4:p.Gly9174=
|
|
NM_133378.4:c.47013C>T
(TTN)
|
NP_596869.4:p.Gly15671=
|
|
NM_133432.3:c.27897C>T
(TTN)
|
NP_597676.3:p.Gly9299=
|
|
NM_133437.4:c.28098C>T
(TTN)
|
NP_597681.4:p.Gly9366=
|
|
NR_038271.1:n.683-4197G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3918-761G>A
(TTN-AS1)
|
|
|
ENST00000342175.10:c.28098C>T
(TTN)
|
ENSP00000340554.6:p.Gly9366=
|
|
ENST00000342175.11:c.28098C>T
(TTN)
|
ENSP00000340554.6:p.Gly9366=
|
|
ENST00000342992.10:c.47013C>T
(TTN)
|
ENSP00000343764.6:p.Gly15671=
|
|
ENST00000342992.11:c.47013C>T
(TTN)
|
ENSP00000343764.6:p.Gly15671=
|
|
ENST00000359218.10:c.27897C>T
(TTN)
|
ENSP00000352154.5:p.Gly9299=
|
|
ENST00000359218.9:c.27897C>T
(TTN)
|
ENSP00000352154.5:p.Gly9299=
|
|
ENST00000460472.6:c.27522C>T
(TTN)
|
ENSP00000434586.1:p.Gly9174=
|
|
ENST00000591111.5:c.49794C>T
(TTN)
|
ENSP00000465570.1:p.Gly16598=
|
|
ENST00000615779.4:c.49794C>T
(TTN)
|
ENSP00000483597.1:p.Gly16598=
|
|
XM_011511729.1:c.53814C>T
(TTN)
|
XP_011510031.1:p.Gly17938=
|
|
XM_011511730.1:c.27708C>T
(TTN)
|
XP_011510032.1:p.Gly9236=
|
|
XM_011511731.1:c.27567C>T
(TTN)
|
XP_011510033.1:p.Gly9189=
|
|
XM_017004819.1:c.53610C>T
(TTN)
|
XP_016860308.1:p.Gly17870=
|
|
XM_017004820.1:c.49008C>T
(TTN)
|
XP_016860309.1:p.Gly16336=
|
|
XM_017004821.1:c.49005C>T
(TTN)
|
XP_016860310.1:p.Gly16335=
|
|
XM_017004822.1:c.46047C>T
(TTN)
|
XP_016860311.1:p.Gly15349=
|
|
XM_017004823.1:c.27663C>T
(TTN)
|
XP_016860312.1:p.Gly9221=
|
|
XM_024453094.1:c.49158C>T
(TTN)
|
XP_024308862.1:p.Gly16386=
|
|
XM_024453095.1:c.49155C>T
(TTN)
|
XP_024308863.1:p.Gly16385=
|
|
XM_024453096.1:c.48588C>T
(TTN)
|
XP_024308864.1:p.Gly16196=
|
|
XM_024453097.1:c.45930C>T
(TTN)
|
XP_024308865.1:p.Gly15310=
|
|
XM_024453098.1:c.45849C>T
(TTN)
|
XP_024308866.1:p.Gly15283=
|
|
XM_024453099.1:c.27612C>T
(TTN)
|
XP_024308867.1:p.Gly9204=
|
|
XM_024453100.1:c.17466C>T
(TTN)
|
XP_024308868.1:p.Gly5822=
|
