ENST00000342992.11:c.69013C>G
(TTN)
|
ENSP00000343764.6:p.Arg23005Gly
|
|
ENST00000342175.11:c.50098C>G
(TTN)
|
ENSP00000340554.6:p.Arg16700Gly
|
|
ENST00000359218.10:c.49897C>G
(TTN)
|
ENSP00000352154.5:p.Arg16633Gly
|
|
ENST00000342175.10:c.50098C>G
(TTN)
|
ENSP00000340554.6:p.Arg16700Gly
|
|
ENST00000342992.10:c.69013C>G
(TTN)
|
ENSP00000343764.6:p.Arg23005Gly
|
|
ENST00000359218.9:c.49897C>G
(TTN)
|
ENSP00000352154.5:p.Arg16633Gly
|
|
ENST00000460472.6:c.49522C>G
(TTN)
|
ENSP00000434586.1:p.Arg16508Gly
|
|
ENST00000589042.5:c.76717C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg25573Gly
|
|
ENST00000591111.5:c.71794C>G
(TTN)
|
ENSP00000465570.1:p.Arg23932Gly
|
|
ENST00000615779.4:c.71794C>G
(TTN)
|
ENSP00000483597.1:p.Arg23932Gly
|
|
NM_001256850.1:c.71794C>G
(TTN)
|
NP_001243779.1:p.Arg23932Gly
|
|
NM_001267550.2:c.76717C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Arg25573Gly
|
|
NM_003319.4:c.49522C>G
(TTN)
|
NP_003310.4:p.Arg16508Gly
|
|
NM_133378.4:c.69013C>G
(TTN)
|
NP_596869.4:p.Arg23005Gly
|
|
NM_133432.3:c.49897C>G
(TTN)
|
NP_597676.3:p.Arg16633Gly
|
|
NM_133437.4:c.50098C>G
(TTN)
|
NP_597681.4:p.Arg16700Gly
|
|
NR_038271.1:n.447-1885G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13157G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.75814C>G
(TTN)
|
XP_011510031.1:p.Arg25272Gly
|
|
XM_011511730.1:c.49708C>G
(TTN)
|
XP_011510032.1:p.Arg16570Gly
|
|
XM_011511731.1:c.49567C>G
(TTN)
|
XP_011510033.1:p.Arg16523Gly
|
|
XM_017004819.1:c.75610C>G
(TTN)
|
XP_016860308.1:p.Arg25204Gly
|
|
XM_017004820.1:c.71008C>G
(TTN)
|
XP_016860309.1:p.Arg23670Gly
|
|
XM_017004821.1:c.71005C>G
(TTN)
|
XP_016860310.1:p.Arg23669Gly
|
|
XM_017004822.1:c.68047C>G
(TTN)
|
XP_016860311.1:p.Arg22683Gly
|
|
XM_017004823.1:c.49663C>G
(TTN)
|
XP_016860312.1:p.Arg16555Gly
|
|
XM_024453094.1:c.71158C>G
(TTN)
|
XP_024308862.1:p.Arg23720Gly
|
|
XM_024453095.1:c.71155C>G
(TTN)
|
XP_024308863.1:p.Arg23719Gly
|
|
XM_024453096.1:c.70588C>G
(TTN)
|
XP_024308864.1:p.Arg23530Gly
|
|
XM_024453097.1:c.67930C>G
(TTN)
|
XP_024308865.1:p.Arg22644Gly
|
|
XM_024453098.1:c.67849C>G
(TTN)
|
XP_024308866.1:p.Arg22617Gly
|
|
XM_024453099.1:c.49612C>G
(TTN)
|
XP_024308867.1:p.Arg16538Gly
|
|
XM_024453100.1:c.39466C>G
(TTN)
|
XP_024308868.1:p.Arg13156Gly
|
|