ENST00000342992.11:c.50654A>G
(TTN)
|
ENSP00000343764.6:p.Asp16885Gly
|
|
ENST00000342175.11:c.31739A>G
(TTN)
|
ENSP00000340554.6:p.Asp10580Gly
|
|
ENST00000359218.10:c.31538A>G
(TTN)
|
ENSP00000352154.5:p.Asp10513Gly
|
|
ENST00000342175.10:c.31739A>G
(TTN)
|
ENSP00000340554.6:p.Asp10580Gly
|
|
ENST00000342992.10:c.50654A>G
(TTN)
|
ENSP00000343764.6:p.Asp16885Gly
|
|
ENST00000359218.9:c.31538A>G
(TTN)
|
ENSP00000352154.5:p.Asp10513Gly
|
|
ENST00000460472.6:c.31163A>G
(TTN)
|
ENSP00000434586.1:p.Asp10388Gly
|
|
ENST00000589042.5:c.58358A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp19453Gly
|
|
ENST00000591111.5:c.53435A>G
(TTN)
|
ENSP00000465570.1:p.Asp17812Gly
|
|
ENST00000615779.4:c.53435A>G
(TTN)
|
ENSP00000483597.1:p.Asp17812Gly
|
|
NM_001256850.1:c.53435A>G
(TTN)
|
NP_001243779.1:p.Asp17812Gly
|
|
NM_001267550.2:c.58358A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp19453Gly
|
|
NM_003319.4:c.31163A>G
(TTN)
|
NP_003310.4:p.Asp10388Gly
|
|
NM_133378.4:c.50654A>G
(TTN)
|
NP_596869.4:p.Asp16885Gly
|
|
NM_133432.3:c.31538A>G
(TTN)
|
NP_597676.3:p.Asp10513Gly
|
|
NM_133437.4:c.31739A>G
(TTN)
|
NP_597681.4:p.Asp10580Gly
|
|
NR_038271.1:n.597-3561T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+2721T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.57455A>G
(TTN)
|
XP_011510031.1:p.Asp19152Gly
|
|
XM_011511730.1:c.31349A>G
(TTN)
|
XP_011510032.1:p.Asp10450Gly
|
|
XM_011511731.1:c.31208A>G
(TTN)
|
XP_011510033.1:p.Asp10403Gly
|
|
XM_017004819.1:c.57251A>G
(TTN)
|
XP_016860308.1:p.Asp19084Gly
|
|
XM_017004820.1:c.52649A>G
(TTN)
|
XP_016860309.1:p.Asp17550Gly
|
|
XM_017004821.1:c.52646A>G
(TTN)
|
XP_016860310.1:p.Asp17549Gly
|
|
XM_017004822.1:c.49688A>G
(TTN)
|
XP_016860311.1:p.Asp16563Gly
|
|
XM_017004823.1:c.31304A>G
(TTN)
|
XP_016860312.1:p.Asp10435Gly
|
|
XM_024453094.1:c.52799A>G
(TTN)
|
XP_024308862.1:p.Asp17600Gly
|
|
XM_024453095.1:c.52796A>G
(TTN)
|
XP_024308863.1:p.Asp17599Gly
|
|
XM_024453096.1:c.52229A>G
(TTN)
|
XP_024308864.1:p.Asp17410Gly
|
|
XM_024453097.1:c.49571A>G
(TTN)
|
XP_024308865.1:p.Asp16524Gly
|
|
XM_024453098.1:c.49490A>G
(TTN)
|
XP_024308866.1:p.Asp16497Gly
|
|
XM_024453099.1:c.31253A>G
(TTN)
|
XP_024308867.1:p.Asp10418Gly
|
|
XM_024453100.1:c.21107A>G
(TTN)
|
XP_024308868.1:p.Asp7036Gly
|
|