ENST00000342992.11:c.41648C>G
(TTN)
|
ENSP00000343764.6:p.Pro13883Arg
|
|
ENST00000342175.11:c.22733C>G
(TTN)
|
ENSP00000340554.6:p.Pro7578Arg
|
|
ENST00000359218.10:c.22532C>G
(TTN)
|
ENSP00000352154.5:p.Pro7511Arg
|
|
ENST00000342175.10:c.22733C>G
(TTN)
|
ENSP00000340554.6:p.Pro7578Arg
|
|
ENST00000342992.10:c.41648C>G
(TTN)
|
ENSP00000343764.6:p.Pro13883Arg
|
|
ENST00000359218.9:c.22532C>G
(TTN)
|
ENSP00000352154.5:p.Pro7511Arg
|
|
ENST00000460472.6:c.22157C>G
(TTN)
|
ENSP00000434586.1:p.Pro7386Arg
|
|
ENST00000589042.5:c.49352C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro16451Arg
|
|
ENST00000591111.5:c.44429C>G
(TTN)
|
ENSP00000465570.1:p.Pro14810Arg
|
|
ENST00000615779.4:c.44429C>G
(TTN)
|
ENSP00000483597.1:p.Pro14810Arg
|
|
NM_001256850.1:c.44429C>G
(TTN)
|
NP_001243779.1:p.Pro14810Arg
|
|
NM_001267550.2:c.49352C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro16451Arg
|
|
NM_003319.4:c.22157C>G
(TTN)
|
NP_003310.4:p.Pro7386Arg
|
|
NM_133378.4:c.41648C>G
(TTN)
|
NP_596869.4:p.Pro13883Arg
|
|
NM_133432.3:c.22532C>G
(TTN)
|
NP_597676.3:p.Pro7511Arg
|
|
NM_133437.4:c.22733C>G
(TTN)
|
NP_597681.4:p.Pro7578Arg
|
|
NR_038271.1:n.783-104G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.48449C>G
(TTN)
|
XP_011510031.1:p.Pro16150Arg
|
|
XM_011511730.1:c.22343C>G
(TTN)
|
XP_011510032.1:p.Pro7448Arg
|
|
XM_011511731.1:c.22202C>G
(TTN)
|
XP_011510033.1:p.Pro7401Arg
|
|
XM_017004819.1:c.48245C>G
(TTN)
|
XP_016860308.1:p.Pro16082Arg
|
|
XM_017004820.1:c.43643C>G
(TTN)
|
XP_016860309.1:p.Pro14548Arg
|
|
XM_017004821.1:c.43640C>G
(TTN)
|
XP_016860310.1:p.Pro14547Arg
|
|
XM_017004822.1:c.40682C>G
(TTN)
|
XP_016860311.1:p.Pro13561Arg
|
|
XM_017004823.1:c.22298C>G
(TTN)
|
XP_016860312.1:p.Pro7433Arg
|
|
XM_024453094.1:c.43793C>G
(TTN)
|
XP_024308862.1:p.Pro14598Arg
|
|
XM_024453095.1:c.43790C>G
(TTN)
|
XP_024308863.1:p.Pro14597Arg
|
|
XM_024453096.1:c.43223C>G
(TTN)
|
XP_024308864.1:p.Pro14408Arg
|
|
XM_024453097.1:c.40565C>G
(TTN)
|
XP_024308865.1:p.Pro13522Arg
|
|
XM_024453098.1:c.40484C>G
(TTN)
|
XP_024308866.1:p.Pro13495Arg
|
|
XM_024453099.1:c.22247C>G
(TTN)
|
XP_024308867.1:p.Pro7416Arg
|
|
XM_024453100.1:c.12101C>G
(TTN)
|
XP_024308868.1:p.Pro4034Arg
|
|