ENST00000342992.11:c.63536C>A
(TTN)
|
ENSP00000343764.6:p.Ser21179Tyr
|
|
ENST00000342175.11:c.44621C>A
(TTN)
|
ENSP00000340554.6:p.Ser14874Tyr
|
|
ENST00000359218.10:c.44420C>A
(TTN)
|
ENSP00000352154.5:p.Ser14807Tyr
|
|
ENST00000342175.10:c.44621C>A
(TTN)
|
ENSP00000340554.6:p.Ser14874Tyr
|
|
ENST00000342992.10:c.63536C>A
(TTN)
|
ENSP00000343764.6:p.Ser21179Tyr
|
|
ENST00000359218.9:c.44420C>A
(TTN)
|
ENSP00000352154.5:p.Ser14807Tyr
|
|
ENST00000460472.6:c.44045C>A
(TTN)
|
ENSP00000434586.1:p.Ser14682Tyr
|
|
ENST00000589042.5:c.71240C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser23747Tyr
|
|
ENST00000591111.5:c.66317C>A
(TTN)
|
ENSP00000465570.1:p.Ser22106Tyr
|
|
ENST00000615779.4:c.66317C>A
(TTN)
|
ENSP00000483597.1:p.Ser22106Tyr
|
|
NM_001256850.1:c.66317C>A
(TTN)
|
NP_001243779.1:p.Ser22106Tyr
|
|
NM_001267550.2:c.71240C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser23747Tyr
|
|
NM_003319.4:c.44045C>A
(TTN)
|
NP_003310.4:p.Ser14682Tyr
|
|
NM_133378.4:c.63536C>A
(TTN)
|
NP_596869.4:p.Ser21179Tyr
|
|
NM_133432.3:c.44420C>A
(TTN)
|
NP_597676.3:p.Ser14807Tyr
|
|
NM_133437.4:c.44621C>A
(TTN)
|
NP_597681.4:p.Ser14874Tyr
|
|
NR_038271.1:n.596+3443G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-7680G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.70337C>A
(TTN)
|
XP_011510031.1:p.Ser23446Tyr
|
|
XM_011511730.1:c.44231C>A
(TTN)
|
XP_011510032.1:p.Ser14744Tyr
|
|
XM_011511731.1:c.44090C>A
(TTN)
|
XP_011510033.1:p.Ser14697Tyr
|
|
XM_017004819.1:c.70133C>A
(TTN)
|
XP_016860308.1:p.Ser23378Tyr
|
|
XM_017004820.1:c.65531C>A
(TTN)
|
XP_016860309.1:p.Ser21844Tyr
|
|
XM_017004821.1:c.65528C>A
(TTN)
|
XP_016860310.1:p.Ser21843Tyr
|
|
XM_017004822.1:c.62570C>A
(TTN)
|
XP_016860311.1:p.Ser20857Tyr
|
|
XM_017004823.1:c.44186C>A
(TTN)
|
XP_016860312.1:p.Ser14729Tyr
|
|
XM_024453094.1:c.65681C>A
(TTN)
|
XP_024308862.1:p.Ser21894Tyr
|
|
XM_024453095.1:c.65678C>A
(TTN)
|
XP_024308863.1:p.Ser21893Tyr
|
|
XM_024453096.1:c.65111C>A
(TTN)
|
XP_024308864.1:p.Ser21704Tyr
|
|
XM_024453097.1:c.62453C>A
(TTN)
|
XP_024308865.1:p.Ser20818Tyr
|
|
XM_024453098.1:c.62372C>A
(TTN)
|
XP_024308866.1:p.Ser20791Tyr
|
|
XM_024453099.1:c.44135C>A
(TTN)
|
XP_024308867.1:p.Ser14712Tyr
|
|
XM_024453100.1:c.33989C>A
(TTN)
|
XP_024308868.1:p.Ser11330Tyr
|
|