ENST00000342992.11:c.96903A>G
(TTN)
|
ENSP00000343764.6:p.Glu32301=
|
|
ENST00000342175.11:c.77988A>G
(TTN)
|
ENSP00000340554.6:p.Glu25996=
|
|
ENST00000359218.10:c.77787A>G
(TTN)
|
ENSP00000352154.5:p.Glu25929=
|
|
ENST00000342175.10:c.77988A>G
(TTN)
|
ENSP00000340554.6:p.Glu25996=
|
|
ENST00000342992.10:c.96903A>G
(TTN)
|
ENSP00000343764.6:p.Glu32301=
|
|
ENST00000359218.9:c.77787A>G
(TTN)
|
ENSP00000352154.5:p.Glu25929=
|
|
ENST00000460472.6:c.77412A>G
(TTN)
|
ENSP00000434586.1:p.Glu25804=
|
|
ENST00000589042.5:c.104607A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34869=
|
|
ENST00000591111.5:c.99684A>G
(TTN)
|
ENSP00000465570.1:p.Glu33228=
|
|
ENST00000615779.4:c.99684A>G
(TTN)
|
ENSP00000483597.1:p.Glu33228=
|
|
NM_001256850.1:c.99684A>G
(TTN)
|
NP_001243779.1:p.Glu33228=
|
|
NM_001267550.2:c.104607A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34869=
|
|
NM_003319.4:c.77412A>G
(TTN)
|
NP_003310.4:p.Glu25804=
|
|
NM_133378.4:c.96903A>G
(TTN)
|
NP_596869.4:p.Glu32301=
|
|
NM_133432.3:c.77787A>G
(TTN)
|
NP_597676.3:p.Glu25929=
|
|
NM_133437.4:c.77988A>G
(TTN)
|
NP_597681.4:p.Glu25996=
|
|
NR_038271.1:n.446+8372T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3724T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103704A>G
(TTN)
|
XP_011510031.1:p.Glu34568=
|
|
XM_011511730.1:c.77598A>G
(TTN)
|
XP_011510032.1:p.Glu25866=
|
|
XM_011511731.1:c.77457A>G
(TTN)
|
XP_011510033.1:p.Glu25819=
|
|
XM_017004819.1:c.103500A>G
(TTN)
|
XP_016860308.1:p.Glu34500=
|
|
XM_017004820.1:c.98898A>G
(TTN)
|
XP_016860309.1:p.Glu32966=
|
|
XM_017004821.1:c.98895A>G
(TTN)
|
XP_016860310.1:p.Glu32965=
|
|
XM_017004822.1:c.95937A>G
(TTN)
|
XP_016860311.1:p.Glu31979=
|
|
XM_017004823.1:c.77553A>G
(TTN)
|
XP_016860312.1:p.Glu25851=
|
|
XM_024453094.1:c.99048A>G
(TTN)
|
XP_024308862.1:p.Glu33016=
|
|
XM_024453095.1:c.99045A>G
(TTN)
|
XP_024308863.1:p.Glu33015=
|
|
XM_024453096.1:c.98478A>G
(TTN)
|
XP_024308864.1:p.Glu32826=
|
|
XM_024453097.1:c.95820A>G
(TTN)
|
XP_024308865.1:p.Glu31940=
|
|
XM_024453098.1:c.95739A>G
(TTN)
|
XP_024308866.1:p.Glu31913=
|
|
XM_024453099.1:c.77502A>G
(TTN)
|
XP_024308867.1:p.Glu25834=
|
|
XM_024453100.1:c.67356A>G
(TTN)
|
XP_024308868.1:p.Glu22452=
|
|