ENST00000342992.11:c.59054A>G
(TTN)
|
ENSP00000343764.6:p.Lys19685Arg
|
|
ENST00000342175.11:c.40139A>G
(TTN)
|
ENSP00000340554.6:p.Lys13380Arg
|
|
ENST00000359218.10:c.39938A>G
(TTN)
|
ENSP00000352154.5:p.Lys13313Arg
|
|
ENST00000342175.10:c.40139A>G
(TTN)
|
ENSP00000340554.6:p.Lys13380Arg
|
|
ENST00000342992.10:c.59054A>G
(TTN)
|
ENSP00000343764.6:p.Lys19685Arg
|
|
ENST00000359218.9:c.39938A>G
(TTN)
|
ENSP00000352154.5:p.Lys13313Arg
|
|
ENST00000460472.6:c.39563A>G
(TTN)
|
ENSP00000434586.1:p.Lys13188Arg
|
|
ENST00000589042.5:c.66758A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys22253Arg
|
|
ENST00000591111.5:c.61835A>G
(TTN)
|
ENSP00000465570.1:p.Lys20612Arg
|
|
ENST00000615779.4:c.61835A>G
(TTN)
|
ENSP00000483597.1:p.Lys20612Arg
|
|
NM_001256850.1:c.61835A>G
(TTN)
|
NP_001243779.1:p.Lys20612Arg
|
|
NM_001267550.2:c.66758A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Lys22253Arg
|
|
NM_003319.4:c.39563A>G
(TTN)
|
NP_003310.4:p.Lys13188Arg
|
|
NM_133378.4:c.59054A>G
(TTN)
|
NP_596869.4:p.Lys19685Arg
|
|
NM_133432.3:c.39938A>G
(TTN)
|
NP_597676.3:p.Lys13313Arg
|
|
NM_133437.4:c.40139A>G
(TTN)
|
NP_597681.4:p.Lys13380Arg
|
|
NR_038271.1:n.596+10061T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-1062T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.65855A>G
(TTN)
|
XP_011510031.1:p.Lys21952Arg
|
|
XM_011511730.1:c.39749A>G
(TTN)
|
XP_011510032.1:p.Lys13250Arg
|
|
XM_011511731.1:c.39608A>G
(TTN)
|
XP_011510033.1:p.Lys13203Arg
|
|
XM_017004819.1:c.65651A>G
(TTN)
|
XP_016860308.1:p.Lys21884Arg
|
|
XM_017004820.1:c.61049A>G
(TTN)
|
XP_016860309.1:p.Lys20350Arg
|
|
XM_017004821.1:c.61046A>G
(TTN)
|
XP_016860310.1:p.Lys20349Arg
|
|
XM_017004822.1:c.58088A>G
(TTN)
|
XP_016860311.1:p.Lys19363Arg
|
|
XM_017004823.1:c.39704A>G
(TTN)
|
XP_016860312.1:p.Lys13235Arg
|
|
XM_024453094.1:c.61199A>G
(TTN)
|
XP_024308862.1:p.Lys20400Arg
|
|
XM_024453095.1:c.61196A>G
(TTN)
|
XP_024308863.1:p.Lys20399Arg
|
|
XM_024453096.1:c.60629A>G
(TTN)
|
XP_024308864.1:p.Lys20210Arg
|
|
XM_024453097.1:c.57971A>G
(TTN)
|
XP_024308865.1:p.Lys19324Arg
|
|
XM_024453098.1:c.57890A>G
(TTN)
|
XP_024308866.1:p.Lys19297Arg
|
|
XM_024453099.1:c.39653A>G
(TTN)
|
XP_024308867.1:p.Lys13218Arg
|
|
XM_024453100.1:c.29507A>G
(TTN)
|
XP_024308868.1:p.Lys9836Arg
|
|