ENST00000342992.11:c.57373G>C
(TTN)
|
ENSP00000343764.6:p.Gly19125Arg
|
|
ENST00000342175.11:c.38458G>C
(TTN)
|
ENSP00000340554.6:p.Gly12820Arg
|
|
ENST00000359218.10:c.38257G>C
(TTN)
|
ENSP00000352154.5:p.Gly12753Arg
|
|
ENST00000342175.10:c.38458G>C
(TTN)
|
ENSP00000340554.6:p.Gly12820Arg
|
|
ENST00000342992.10:c.57373G>C
(TTN)
|
ENSP00000343764.6:p.Gly19125Arg
|
|
ENST00000359218.9:c.38257G>C
(TTN)
|
ENSP00000352154.5:p.Gly12753Arg
|
|
ENST00000460472.6:c.37882G>C
(TTN)
|
ENSP00000434586.1:p.Gly12628Arg
|
|
ENST00000589042.5:c.65077G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly21693Arg
|
|
ENST00000591111.5:c.60154G>C
(TTN)
|
ENSP00000465570.1:p.Gly20052Arg
|
|
ENST00000615779.4:c.60154G>C
(TTN)
|
ENSP00000483597.1:p.Gly20052Arg
|
|
NM_001256850.1:c.60154G>C
(TTN)
|
NP_001243779.1:p.Gly20052Arg
|
|
NM_001267550.2:c.65077G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly21693Arg
|
|
NM_003319.4:c.37882G>C
(TTN)
|
NP_003310.4:p.Gly12628Arg
|
|
NM_133378.4:c.57373G>C
(TTN)
|
NP_596869.4:p.Gly19125Arg
|
|
NM_133432.3:c.38257G>C
(TTN)
|
NP_597676.3:p.Gly12753Arg
|
|
NM_133437.4:c.38458G>C
(TTN)
|
NP_597681.4:p.Gly12820Arg
|
|
NR_038271.1:n.596+13025C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2768-99C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.64174G>C
(TTN)
|
XP_011510031.1:p.Gly21392Arg
|
|
XM_011511730.1:c.38068G>C
(TTN)
|
XP_011510032.1:p.Gly12690Arg
|
|
XM_011511731.1:c.37927G>C
(TTN)
|
XP_011510033.1:p.Gly12643Arg
|
|
XM_017004819.1:c.63970G>C
(TTN)
|
XP_016860308.1:p.Gly21324Arg
|
|
XM_017004820.1:c.59368G>C
(TTN)
|
XP_016860309.1:p.Gly19790Arg
|
|
XM_017004821.1:c.59365G>C
(TTN)
|
XP_016860310.1:p.Gly19789Arg
|
|
XM_017004822.1:c.56407G>C
(TTN)
|
XP_016860311.1:p.Gly18803Arg
|
|
XM_017004823.1:c.38023G>C
(TTN)
|
XP_016860312.1:p.Gly12675Arg
|
|
XM_024453094.1:c.59518G>C
(TTN)
|
XP_024308862.1:p.Gly19840Arg
|
|
XM_024453095.1:c.59515G>C
(TTN)
|
XP_024308863.1:p.Gly19839Arg
|
|
XM_024453096.1:c.58948G>C
(TTN)
|
XP_024308864.1:p.Gly19650Arg
|
|
XM_024453097.1:c.56290G>C
(TTN)
|
XP_024308865.1:p.Gly18764Arg
|
|
XM_024453098.1:c.56209G>C
(TTN)
|
XP_024308866.1:p.Gly18737Arg
|
|
XM_024453099.1:c.37972G>C
(TTN)
|
XP_024308867.1:p.Gly12658Arg
|
|
XM_024453100.1:c.27826G>C
(TTN)
|
XP_024308868.1:p.Gly9276Arg
|
|