ENST00000342992.11:c.39065C>G
(TTN)
|
ENSP00000343764.6:p.Pro13022Arg
|
|
ENST00000342175.11:c.20150C>G
(TTN)
|
ENSP00000340554.6:p.Pro6717Arg
|
|
ENST00000359218.10:c.19949C>G
(TTN)
|
ENSP00000352154.5:p.Pro6650Arg
|
|
ENST00000342175.10:c.20150C>G
(TTN)
|
ENSP00000340554.6:p.Pro6717Arg
|
|
ENST00000342992.10:c.39065C>G
(TTN)
|
ENSP00000343764.6:p.Pro13022Arg
|
|
ENST00000359218.9:c.19949C>G
(TTN)
|
ENSP00000352154.5:p.Pro6650Arg
|
|
ENST00000460472.6:c.19574C>G
(TTN)
|
ENSP00000434586.1:p.Pro6525Arg
|
|
ENST00000589042.5:c.46769C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro15590Arg
|
|
ENST00000591111.5:c.41846C>G
(TTN)
|
ENSP00000465570.1:p.Pro13949Arg
|
|
ENST00000615779.4:c.41846C>G
(TTN)
|
ENSP00000483597.1:p.Pro13949Arg
|
|
NM_001256850.1:c.41846C>G
(TTN)
|
NP_001243779.1:p.Pro13949Arg
|
|
NM_001267550.2:c.46769C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro15590Arg
|
|
NM_003319.4:c.19574C>G
(TTN)
|
NP_003310.4:p.Pro6525Arg
|
|
NM_133378.4:c.39065C>G
(TTN)
|
NP_596869.4:p.Pro13022Arg
|
|
NM_133432.3:c.19949C>G
(TTN)
|
NP_597676.3:p.Pro6650Arg
|
|
NM_133437.4:c.20150C>G
(TTN)
|
NP_597681.4:p.Pro6717Arg
|
|
NR_038271.1:n.1605-972G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.45866C>G
(TTN)
|
XP_011510031.1:p.Pro15289Arg
|
|
XM_011511730.1:c.19760C>G
(TTN)
|
XP_011510032.1:p.Pro6587Arg
|
|
XM_011511731.1:c.19619C>G
(TTN)
|
XP_011510033.1:p.Pro6540Arg
|
|
XM_017004819.1:c.45662C>G
(TTN)
|
XP_016860308.1:p.Pro15221Arg
|
|
XM_017004820.1:c.41060C>G
(TTN)
|
XP_016860309.1:p.Pro13687Arg
|
|
XM_017004821.1:c.41057C>G
(TTN)
|
XP_016860310.1:p.Pro13686Arg
|
|
XM_017004822.1:c.38099C>G
(TTN)
|
XP_016860311.1:p.Pro12700Arg
|
|
XM_017004823.1:c.19715C>G
(TTN)
|
XP_016860312.1:p.Pro6572Arg
|
|
XM_024453094.1:c.41210C>G
(TTN)
|
XP_024308862.1:p.Pro13737Arg
|
|
XM_024453095.1:c.41207C>G
(TTN)
|
XP_024308863.1:p.Pro13736Arg
|
|
XM_024453096.1:c.40640C>G
(TTN)
|
XP_024308864.1:p.Pro13547Arg
|
|
XM_024453097.1:c.37982C>G
(TTN)
|
XP_024308865.1:p.Pro12661Arg
|
|
XM_024453098.1:c.37901C>G
(TTN)
|
XP_024308866.1:p.Pro12634Arg
|
|
XM_024453099.1:c.19664C>G
(TTN)
|
XP_024308867.1:p.Pro6555Arg
|
|
XM_024453100.1:c.9518C>G
(TTN)
|
XP_024308868.1:p.Pro3173Arg
|
|