ENST00000342992.11:c.53110C>G
(TTN)
|
ENSP00000343764.6:p.Pro17704Ala
|
|
ENST00000342175.11:c.34195C>G
(TTN)
|
ENSP00000340554.6:p.Pro11399Ala
|
|
ENST00000359218.10:c.33994C>G
(TTN)
|
ENSP00000352154.5:p.Pro11332Ala
|
|
ENST00000342175.10:c.34195C>G
(TTN)
|
ENSP00000340554.6:p.Pro11399Ala
|
|
ENST00000342992.10:c.53110C>G
(TTN)
|
ENSP00000343764.6:p.Pro17704Ala
|
|
ENST00000359218.9:c.33994C>G
(TTN)
|
ENSP00000352154.5:p.Pro11332Ala
|
|
ENST00000460472.6:c.33619C>G
(TTN)
|
ENSP00000434586.1:p.Pro11207Ala
|
|
ENST00000589042.5:c.60814C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro20272Ala
|
|
ENST00000591111.5:c.55891C>G
(TTN)
|
ENSP00000465570.1:p.Pro18631Ala
|
|
ENST00000615779.4:c.55891C>G
(TTN)
|
ENSP00000483597.1:p.Pro18631Ala
|
|
NM_001256850.1:c.55891C>G
(TTN)
|
NP_001243779.1:p.Pro18631Ala
|
|
NM_001267550.2:c.60814C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro20272Ala
|
|
NM_003319.4:c.33619C>G
(TTN)
|
NP_003310.4:p.Pro11207Ala
|
|
NM_133378.4:c.53110C>G
(TTN)
|
NP_596869.4:p.Pro17704Ala
|
|
NM_133432.3:c.33994C>G
(TTN)
|
NP_597676.3:p.Pro11332Ala
|
|
NM_133437.4:c.34195C>G
(TTN)
|
NP_597681.4:p.Pro11399Ala
|
|
NR_038271.1:n.597-6685G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-228G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.59911C>G
(TTN)
|
XP_011510031.1:p.Pro19971Ala
|
|
XM_011511730.1:c.33805C>G
(TTN)
|
XP_011510032.1:p.Pro11269Ala
|
|
XM_011511731.1:c.33664C>G
(TTN)
|
XP_011510033.1:p.Pro11222Ala
|
|
XM_017004819.1:c.59707C>G
(TTN)
|
XP_016860308.1:p.Pro19903Ala
|
|
XM_017004820.1:c.55105C>G
(TTN)
|
XP_016860309.1:p.Pro18369Ala
|
|
XM_017004821.1:c.55102C>G
(TTN)
|
XP_016860310.1:p.Pro18368Ala
|
|
XM_017004822.1:c.52144C>G
(TTN)
|
XP_016860311.1:p.Pro17382Ala
|
|
XM_017004823.1:c.33760C>G
(TTN)
|
XP_016860312.1:p.Pro11254Ala
|
|
XM_024453094.1:c.55255C>G
(TTN)
|
XP_024308862.1:p.Pro18419Ala
|
|
XM_024453095.1:c.55252C>G
(TTN)
|
XP_024308863.1:p.Pro18418Ala
|
|
XM_024453096.1:c.54685C>G
(TTN)
|
XP_024308864.1:p.Pro18229Ala
|
|
XM_024453097.1:c.52027C>G
(TTN)
|
XP_024308865.1:p.Pro17343Ala
|
|
XM_024453098.1:c.51946C>G
(TTN)
|
XP_024308866.1:p.Pro17316Ala
|
|
XM_024453099.1:c.33709C>G
(TTN)
|
XP_024308867.1:p.Pro11237Ala
|
|
XM_024453100.1:c.23563C>G
(TTN)
|
XP_024308868.1:p.Pro7855Ala
|
|