ENST00000342992.11:c.69496A>G
(TTN)
|
ENSP00000343764.6:p.Ile23166Val
|
|
ENST00000342175.11:c.50581A>G
(TTN)
|
ENSP00000340554.6:p.Ile16861Val
|
|
ENST00000359218.10:c.50380A>G
(TTN)
|
ENSP00000352154.5:p.Ile16794Val
|
|
ENST00000342175.10:c.50581A>G
(TTN)
|
ENSP00000340554.6:p.Ile16861Val
|
|
ENST00000342992.10:c.69496A>G
(TTN)
|
ENSP00000343764.6:p.Ile23166Val
|
|
ENST00000359218.9:c.50380A>G
(TTN)
|
ENSP00000352154.5:p.Ile16794Val
|
|
ENST00000460472.6:c.50005A>G
(TTN)
|
ENSP00000434586.1:p.Ile16669Val
|
|
ENST00000589042.5:c.77200A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile25734Val
|
|
ENST00000591111.5:c.72277A>G
(TTN)
|
ENSP00000465570.1:p.Ile24093Val
|
|
ENST00000615779.4:c.72277A>G
(TTN)
|
ENSP00000483597.1:p.Ile24093Val
|
|
NM_001256850.1:c.72277A>G
(TTN)
|
NP_001243779.1:p.Ile24093Val
|
|
NM_001267550.2:c.77200A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ile25734Val
|
|
NM_003319.4:c.50005A>G
(TTN)
|
NP_003310.4:p.Ile16669Val
|
|
NM_133378.4:c.69496A>G
(TTN)
|
NP_596869.4:p.Ile23166Val
|
|
NM_133432.3:c.50380A>G
(TTN)
|
NP_597676.3:p.Ile16794Val
|
|
NM_133437.4:c.50581A>G
(TTN)
|
NP_597681.4:p.Ile16861Val
|
|
NR_038271.1:n.447-2368T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13640T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.76297A>G
(TTN)
|
XP_011510031.1:p.Ile25433Val
|
|
XM_011511730.1:c.50191A>G
(TTN)
|
XP_011510032.1:p.Ile16731Val
|
|
XM_011511731.1:c.50050A>G
(TTN)
|
XP_011510033.1:p.Ile16684Val
|
|
XM_017004819.1:c.76093A>G
(TTN)
|
XP_016860308.1:p.Ile25365Val
|
|
XM_017004820.1:c.71491A>G
(TTN)
|
XP_016860309.1:p.Ile23831Val
|
|
XM_017004821.1:c.71488A>G
(TTN)
|
XP_016860310.1:p.Ile23830Val
|
|
XM_017004822.1:c.68530A>G
(TTN)
|
XP_016860311.1:p.Ile22844Val
|
|
XM_017004823.1:c.50146A>G
(TTN)
|
XP_016860312.1:p.Ile16716Val
|
|
XM_024453094.1:c.71641A>G
(TTN)
|
XP_024308862.1:p.Ile23881Val
|
|
XM_024453095.1:c.71638A>G
(TTN)
|
XP_024308863.1:p.Ile23880Val
|
|
XM_024453096.1:c.71071A>G
(TTN)
|
XP_024308864.1:p.Ile23691Val
|
|
XM_024453097.1:c.68413A>G
(TTN)
|
XP_024308865.1:p.Ile22805Val
|
|
XM_024453098.1:c.68332A>G
(TTN)
|
XP_024308866.1:p.Ile22778Val
|
|
XM_024453099.1:c.50095A>G
(TTN)
|
XP_024308867.1:p.Ile16699Val
|
|
XM_024453100.1:c.39949A>G
(TTN)
|
XP_024308868.1:p.Ile13317Val
|
|