ENST00000342992.11:c.96706A>G
(TTN)
|
ENSP00000343764.6:p.Arg32236Gly
|
|
ENST00000342175.11:c.77791A>G
(TTN)
|
ENSP00000340554.6:p.Arg25931Gly
|
|
ENST00000359218.10:c.77590A>G
(TTN)
|
ENSP00000352154.5:p.Arg25864Gly
|
|
ENST00000342175.10:c.77791A>G
(TTN)
|
ENSP00000340554.6:p.Arg25931Gly
|
|
ENST00000342992.10:c.96706A>G
(TTN)
|
ENSP00000343764.6:p.Arg32236Gly
|
|
ENST00000359218.9:c.77590A>G
(TTN)
|
ENSP00000352154.5:p.Arg25864Gly
|
|
ENST00000460472.6:c.77215A>G
(TTN)
|
ENSP00000434586.1:p.Arg25739Gly
|
|
ENST00000589042.5:c.104410A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg34804Gly
|
|
ENST00000591111.5:c.99487A>G
(TTN)
|
ENSP00000465570.1:p.Arg33163Gly
|
|
ENST00000615779.4:c.99487A>G
(TTN)
|
ENSP00000483597.1:p.Arg33163Gly
|
|
NM_001256850.1:c.99487A>G
(TTN)
|
NP_001243779.1:p.Arg33163Gly
|
|
NM_001267550.2:c.104410A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Arg34804Gly
|
|
NM_003319.4:c.77215A>G
(TTN)
|
NP_003310.4:p.Arg25739Gly
|
|
NM_133378.4:c.96706A>G
(TTN)
|
NP_596869.4:p.Arg32236Gly
|
|
NM_133432.3:c.77590A>G
(TTN)
|
NP_597676.3:p.Arg25864Gly
|
|
NM_133437.4:c.77791A>G
(TTN)
|
NP_597681.4:p.Arg25931Gly
|
|
NR_038271.1:n.446+8569T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3527T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103507A>G
(TTN)
|
XP_011510031.1:p.Arg34503Gly
|
|
XM_011511730.1:c.77401A>G
(TTN)
|
XP_011510032.1:p.Arg25801Gly
|
|
XM_011511731.1:c.77260A>G
(TTN)
|
XP_011510033.1:p.Arg25754Gly
|
|
XM_017004819.1:c.103303A>G
(TTN)
|
XP_016860308.1:p.Arg34435Gly
|
|
XM_017004820.1:c.98701A>G
(TTN)
|
XP_016860309.1:p.Arg32901Gly
|
|
XM_017004821.1:c.98698A>G
(TTN)
|
XP_016860310.1:p.Arg32900Gly
|
|
XM_017004822.1:c.95740A>G
(TTN)
|
XP_016860311.1:p.Arg31914Gly
|
|
XM_017004823.1:c.77356A>G
(TTN)
|
XP_016860312.1:p.Arg25786Gly
|
|
XM_024453094.1:c.98851A>G
(TTN)
|
XP_024308862.1:p.Arg32951Gly
|
|
XM_024453095.1:c.98848A>G
(TTN)
|
XP_024308863.1:p.Arg32950Gly
|
|
XM_024453096.1:c.98281A>G
(TTN)
|
XP_024308864.1:p.Arg32761Gly
|
|
XM_024453097.1:c.95623A>G
(TTN)
|
XP_024308865.1:p.Arg31875Gly
|
|
XM_024453098.1:c.95542A>G
(TTN)
|
XP_024308866.1:p.Arg31848Gly
|
|
XM_024453099.1:c.77305A>G
(TTN)
|
XP_024308867.1:p.Arg25769Gly
|
|
XM_024453100.1:c.67159A>G
(TTN)
|
XP_024308868.1:p.Arg22387Gly
|
|