ENST00000342992.11:c.57262C>G
(TTN)
|
ENSP00000343764.6:p.Pro19088Ala
|
|
ENST00000342175.11:c.38347C>G
(TTN)
|
ENSP00000340554.6:p.Pro12783Ala
|
|
ENST00000359218.10:c.38146C>G
(TTN)
|
ENSP00000352154.5:p.Pro12716Ala
|
|
ENST00000342175.10:c.38347C>G
(TTN)
|
ENSP00000340554.6:p.Pro12783Ala
|
|
ENST00000342992.10:c.57262C>G
(TTN)
|
ENSP00000343764.6:p.Pro19088Ala
|
|
ENST00000359218.9:c.38146C>G
(TTN)
|
ENSP00000352154.5:p.Pro12716Ala
|
|
ENST00000460472.6:c.37771C>G
(TTN)
|
ENSP00000434586.1:p.Pro12591Ala
|
|
ENST00000589042.5:c.64966C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro21656Ala
|
|
ENST00000591111.5:c.60043C>G
(TTN)
|
ENSP00000465570.1:p.Pro20015Ala
|
|
ENST00000615779.4:c.60043C>G
(TTN)
|
ENSP00000483597.1:p.Pro20015Ala
|
|
NM_001256850.1:c.60043C>G
(TTN)
|
NP_001243779.1:p.Pro20015Ala
|
|
NM_001267550.2:c.64966C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro21656Ala
|
|
NM_003319.4:c.37771C>G
(TTN)
|
NP_003310.4:p.Pro12591Ala
|
|
NM_133378.4:c.57262C>G
(TTN)
|
NP_596869.4:p.Pro19088Ala
|
|
NM_133432.3:c.38146C>G
(TTN)
|
NP_597676.3:p.Pro12716Ala
|
|
NM_133437.4:c.38347C>G
(TTN)
|
NP_597681.4:p.Pro12783Ala
|
|
NR_038271.1:n.597-12921G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2870G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.64063C>G
(TTN)
|
XP_011510031.1:p.Pro21355Ala
|
|
XM_011511730.1:c.37957C>G
(TTN)
|
XP_011510032.1:p.Pro12653Ala
|
|
XM_011511731.1:c.37816C>G
(TTN)
|
XP_011510033.1:p.Pro12606Ala
|
|
XM_017004819.1:c.63859C>G
(TTN)
|
XP_016860308.1:p.Pro21287Ala
|
|
XM_017004820.1:c.59257C>G
(TTN)
|
XP_016860309.1:p.Pro19753Ala
|
|
XM_017004821.1:c.59254C>G
(TTN)
|
XP_016860310.1:p.Pro19752Ala
|
|
XM_017004822.1:c.56296C>G
(TTN)
|
XP_016860311.1:p.Pro18766Ala
|
|
XM_017004823.1:c.37912C>G
(TTN)
|
XP_016860312.1:p.Pro12638Ala
|
|
XM_024453094.1:c.59407C>G
(TTN)
|
XP_024308862.1:p.Pro19803Ala
|
|
XM_024453095.1:c.59404C>G
(TTN)
|
XP_024308863.1:p.Pro19802Ala
|
|
XM_024453096.1:c.58837C>G
(TTN)
|
XP_024308864.1:p.Pro19613Ala
|
|
XM_024453097.1:c.56179C>G
(TTN)
|
XP_024308865.1:p.Pro18727Ala
|
|
XM_024453098.1:c.56098C>G
(TTN)
|
XP_024308866.1:p.Pro18700Ala
|
|
XM_024453099.1:c.37861C>G
(TTN)
|
XP_024308867.1:p.Pro12621Ala
|
|
XM_024453100.1:c.27715C>G
(TTN)
|
XP_024308868.1:p.Pro9239Ala
|
|