ENST00000342992.11:c.87318G>A
(TTN)
|
ENSP00000343764.6:p.Val29106=
|
|
ENST00000342175.11:c.68403G>A
(TTN)
|
ENSP00000340554.6:p.Val22801=
|
|
ENST00000359218.10:c.68202G>A
(TTN)
|
ENSP00000352154.5:p.Val22734=
|
|
ENST00000342175.10:c.68403G>A
(TTN)
|
ENSP00000340554.6:p.Val22801=
|
|
ENST00000342992.10:c.87318G>A
(TTN)
|
ENSP00000343764.6:p.Val29106=
|
|
ENST00000359218.9:c.68202G>A
(TTN)
|
ENSP00000352154.5:p.Val22734=
|
|
ENST00000460472.6:c.67827G>A
(TTN)
|
ENSP00000434586.1:p.Val22609=
|
|
ENST00000589042.5:c.95022G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val31674=
|
|
ENST00000591111.5:c.90099G>A
(TTN)
|
ENSP00000465570.1:p.Val30033=
|
|
ENST00000615779.4:c.90099G>A
(TTN)
|
ENSP00000483597.1:p.Val30033=
|
|
NM_001256850.1:c.90099G>A
(TTN)
|
NP_001243779.1:p.Val30033=
|
|
NM_001267550.2:c.95022G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Val31674=
|
|
NM_003319.4:c.67827G>A
(TTN)
|
NP_003310.4:p.Val22609=
|
|
NM_133378.4:c.87318G>A
(TTN)
|
NP_596869.4:p.Val29106=
|
|
NM_133432.3:c.68202G>A
(TTN)
|
NP_597676.3:p.Val22734=
|
|
NM_133437.4:c.68403G>A
(TTN)
|
NP_597681.4:p.Val22801=
|
|
NR_038271.1:n.446+22673C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+3948C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.94119G>A
(TTN)
|
XP_011510031.1:p.Val31373=
|
|
XM_011511730.1:c.68013G>A
(TTN)
|
XP_011510032.1:p.Val22671=
|
|
XM_011511731.1:c.67872G>A
(TTN)
|
XP_011510033.1:p.Val22624=
|
|
XM_017004819.1:c.93915G>A
(TTN)
|
XP_016860308.1:p.Val31305=
|
|
XM_017004820.1:c.89313G>A
(TTN)
|
XP_016860309.1:p.Val29771=
|
|
XM_017004821.1:c.89310G>A
(TTN)
|
XP_016860310.1:p.Val29770=
|
|
XM_017004822.1:c.86352G>A
(TTN)
|
XP_016860311.1:p.Val28784=
|
|
XM_017004823.1:c.67968G>A
(TTN)
|
XP_016860312.1:p.Val22656=
|
|
XM_024453094.1:c.89463G>A
(TTN)
|
XP_024308862.1:p.Val29821=
|
|
XM_024453095.1:c.89460G>A
(TTN)
|
XP_024308863.1:p.Val29820=
|
|
XM_024453096.1:c.88893G>A
(TTN)
|
XP_024308864.1:p.Val29631=
|
|
XM_024453097.1:c.86235G>A
(TTN)
|
XP_024308865.1:p.Val28745=
|
|
XM_024453098.1:c.86154G>A
(TTN)
|
XP_024308866.1:p.Val28718=
|
|
XM_024453099.1:c.67917G>A
(TTN)
|
XP_024308867.1:p.Val22639=
|
|
XM_024453100.1:c.57771G>A
(TTN)
|
XP_024308868.1:p.Val19257=
|
|