ENST00000342992.11:c.52228C>G
(TTN)
|
ENSP00000343764.6:p.Pro17410Ala
|
|
ENST00000342175.11:c.33313C>G
(TTN)
|
ENSP00000340554.6:p.Pro11105Ala
|
|
ENST00000359218.10:c.33112C>G
(TTN)
|
ENSP00000352154.5:p.Pro11038Ala
|
|
ENST00000342175.10:c.33313C>G
(TTN)
|
ENSP00000340554.6:p.Pro11105Ala
|
|
ENST00000342992.10:c.52228C>G
(TTN)
|
ENSP00000343764.6:p.Pro17410Ala
|
|
ENST00000359218.9:c.33112C>G
(TTN)
|
ENSP00000352154.5:p.Pro11038Ala
|
|
ENST00000460472.6:c.32737C>G
(TTN)
|
ENSP00000434586.1:p.Pro10913Ala
|
|
ENST00000589042.5:c.59932C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19978Ala
|
|
ENST00000591111.5:c.55009C>G
(TTN)
|
ENSP00000465570.1:p.Pro18337Ala
|
|
ENST00000615779.4:c.55009C>G
(TTN)
|
ENSP00000483597.1:p.Pro18337Ala
|
|
NM_001256850.1:c.55009C>G
(TTN)
|
NP_001243779.1:p.Pro18337Ala
|
|
NM_001267550.2:c.59932C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19978Ala
|
|
NM_003319.4:c.32737C>G
(TTN)
|
NP_003310.4:p.Pro10913Ala
|
|
NM_133378.4:c.52228C>G
(TTN)
|
NP_596869.4:p.Pro17410Ala
|
|
NM_133432.3:c.33112C>G
(TTN)
|
NP_597676.3:p.Pro11038Ala
|
|
NM_133437.4:c.33313C>G
(TTN)
|
NP_597681.4:p.Pro11105Ala
|
|
NR_038271.1:n.597-5709G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+573G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.59029C>G
(TTN)
|
XP_011510031.1:p.Pro19677Ala
|
|
XM_011511730.1:c.32923C>G
(TTN)
|
XP_011510032.1:p.Pro10975Ala
|
|
XM_011511731.1:c.32782C>G
(TTN)
|
XP_011510033.1:p.Pro10928Ala
|
|
XM_017004819.1:c.58825C>G
(TTN)
|
XP_016860308.1:p.Pro19609Ala
|
|
XM_017004820.1:c.54223C>G
(TTN)
|
XP_016860309.1:p.Pro18075Ala
|
|
XM_017004821.1:c.54220C>G
(TTN)
|
XP_016860310.1:p.Pro18074Ala
|
|
XM_017004822.1:c.51262C>G
(TTN)
|
XP_016860311.1:p.Pro17088Ala
|
|
XM_017004823.1:c.32878C>G
(TTN)
|
XP_016860312.1:p.Pro10960Ala
|
|
XM_024453094.1:c.54373C>G
(TTN)
|
XP_024308862.1:p.Pro18125Ala
|
|
XM_024453095.1:c.54370C>G
(TTN)
|
XP_024308863.1:p.Pro18124Ala
|
|
XM_024453096.1:c.53803C>G
(TTN)
|
XP_024308864.1:p.Pro17935Ala
|
|
XM_024453097.1:c.51145C>G
(TTN)
|
XP_024308865.1:p.Pro17049Ala
|
|
XM_024453098.1:c.51064C>G
(TTN)
|
XP_024308866.1:p.Pro17022Ala
|
|
XM_024453099.1:c.32827C>G
(TTN)
|
XP_024308867.1:p.Pro10943Ala
|
|
XM_024453100.1:c.22681C>G
(TTN)
|
XP_024308868.1:p.Pro7561Ala
|
|