ENST00000342992.11:c.44117C>A
(TTN)
|
ENSP00000343764.6:p.Ser14706Ter
|
|
ENST00000342175.11:c.25202C>A
(TTN)
|
ENSP00000340554.6:p.Ser8401Ter
|
|
ENST00000359218.10:c.25001C>A
(TTN)
|
ENSP00000352154.5:p.Ser8334Ter
|
|
ENST00000342175.10:c.25202C>A
(TTN)
|
ENSP00000340554.6:p.Ser8401Ter
|
|
ENST00000342992.10:c.44117C>A
(TTN)
|
ENSP00000343764.6:p.Ser14706Ter
|
|
ENST00000359218.9:c.25001C>A
(TTN)
|
ENSP00000352154.5:p.Ser8334Ter
|
|
ENST00000460472.6:c.24626C>A
(TTN)
|
ENSP00000434586.1:p.Ser8209Ter
|
|
ENST00000589042.5:c.51821C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser17274Ter
|
|
ENST00000591111.5:c.46898C>A
(TTN)
|
ENSP00000465570.1:p.Ser15633Ter
|
|
ENST00000615779.4:c.46898C>A
(TTN)
|
ENSP00000483597.1:p.Ser15633Ter
|
|
NM_001256850.1:c.46898C>A
(TTN)
|
NP_001243779.1:p.Ser15633Ter
|
|
NM_001267550.2:c.51821C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser17274Ter
|
|
NM_003319.4:c.24626C>A
(TTN)
|
NP_003310.4:p.Ser8209Ter
|
|
NM_133378.4:c.44117C>A
(TTN)
|
NP_596869.4:p.Ser14706Ter
|
|
NM_133432.3:c.25001C>A
(TTN)
|
NP_597676.3:p.Ser8334Ter
|
|
NM_133437.4:c.25202C>A
(TTN)
|
NP_597681.4:p.Ser8401Ter
|
|
NR_038271.1:n.782+1223G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.50918C>A
(TTN)
|
XP_011510031.1:p.Ser16973Ter
|
|
XM_011511730.1:c.24812C>A
(TTN)
|
XP_011510032.1:p.Ser8271Ter
|
|
XM_011511731.1:c.24671C>A
(TTN)
|
XP_011510033.1:p.Ser8224Ter
|
|
XM_017004819.1:c.50714C>A
(TTN)
|
XP_016860308.1:p.Ser16905Ter
|
|
XM_017004820.1:c.46112C>A
(TTN)
|
XP_016860309.1:p.Ser15371Ter
|
|
XM_017004821.1:c.46109C>A
(TTN)
|
XP_016860310.1:p.Ser15370Ter
|
|
XM_017004822.1:c.43151C>A
(TTN)
|
XP_016860311.1:p.Ser14384Ter
|
|
XM_017004823.1:c.24767C>A
(TTN)
|
XP_016860312.1:p.Ser8256Ter
|
|
XM_024453094.1:c.46262C>A
(TTN)
|
XP_024308862.1:p.Ser15421Ter
|
|
XM_024453095.1:c.46259C>A
(TTN)
|
XP_024308863.1:p.Ser15420Ter
|
|
XM_024453096.1:c.45692C>A
(TTN)
|
XP_024308864.1:p.Ser15231Ter
|
|
XM_024453097.1:c.43034C>A
(TTN)
|
XP_024308865.1:p.Ser14345Ter
|
|
XM_024453098.1:c.42953C>A
(TTN)
|
XP_024308866.1:p.Ser14318Ter
|
|
XM_024453099.1:c.24716C>A
(TTN)
|
XP_024308867.1:p.Ser8239Ter
|
|
XM_024453100.1:c.14570C>A
(TTN)
|
XP_024308868.1:p.Ser4857Ter
|
|