ENST00000342992.11:c.98436G>A
(TTN)
|
ENSP00000343764.6:p.Lys32812=
|
|
ENST00000342175.11:c.79521G>A
(TTN)
|
ENSP00000340554.6:p.Lys26507=
|
|
ENST00000359218.10:c.79320G>A
(TTN)
|
ENSP00000352154.5:p.Lys26440=
|
|
ENST00000342175.10:c.79521G>A
(TTN)
|
ENSP00000340554.6:p.Lys26507=
|
|
ENST00000342992.10:c.98436G>A
(TTN)
|
ENSP00000343764.6:p.Lys32812=
|
|
ENST00000359218.9:c.79320G>A
(TTN)
|
ENSP00000352154.5:p.Lys26440=
|
|
ENST00000460472.6:c.78945G>A
(TTN)
|
ENSP00000434586.1:p.Lys26315=
|
|
ENST00000589042.5:c.106140G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys35380=
|
|
ENST00000591111.5:c.101217G>A
(TTN)
|
ENSP00000465570.1:p.Lys33739=
|
|
ENST00000615779.4:c.101217G>A
(TTN)
|
ENSP00000483597.1:p.Lys33739=
|
|
NM_001256850.1:c.101217G>A
(TTN)
|
NP_001243779.1:p.Lys33739=
|
|
NM_001267550.2:c.106140G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Lys35380=
|
|
NM_003319.4:c.78945G>A
(TTN)
|
NP_003310.4:p.Lys26315=
|
|
NM_133378.4:c.98436G>A
(TTN)
|
NP_596869.4:p.Lys32812=
|
|
NM_133432.3:c.79320G>A
(TTN)
|
NP_597676.3:p.Lys26440=
|
|
NM_133437.4:c.79521G>A
(TTN)
|
NP_597681.4:p.Lys26507=
|
|
NR_038271.1:n.446+6839C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5257C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105237G>A
(TTN)
|
XP_011510031.1:p.Lys35079=
|
|
XM_011511730.1:c.79131G>A
(TTN)
|
XP_011510032.1:p.Lys26377=
|
|
XM_011511731.1:c.78990G>A
(TTN)
|
XP_011510033.1:p.Lys26330=
|
|
XM_017004819.1:c.105033G>A
(TTN)
|
XP_016860308.1:p.Lys35011=
|
|
XM_017004820.1:c.100431G>A
(TTN)
|
XP_016860309.1:p.Lys33477=
|
|
XM_017004821.1:c.100428G>A
(TTN)
|
XP_016860310.1:p.Lys33476=
|
|
XM_017004822.1:c.97470G>A
(TTN)
|
XP_016860311.1:p.Lys32490=
|
|
XM_017004823.1:c.79086G>A
(TTN)
|
XP_016860312.1:p.Lys26362=
|
|
XM_024453094.1:c.100581G>A
(TTN)
|
XP_024308862.1:p.Lys33527=
|
|
XM_024453095.1:c.100578G>A
(TTN)
|
XP_024308863.1:p.Lys33526=
|
|
XM_024453096.1:c.100011G>A
(TTN)
|
XP_024308864.1:p.Lys33337=
|
|
XM_024453097.1:c.97353G>A
(TTN)
|
XP_024308865.1:p.Lys32451=
|
|
XM_024453098.1:c.97272G>A
(TTN)
|
XP_024308866.1:p.Lys32424=
|
|
XM_024453099.1:c.79035G>A
(TTN)
|
XP_024308867.1:p.Lys26345=
|
|
XM_024453100.1:c.68889G>A
(TTN)
|
XP_024308868.1:p.Lys22963=
|
|