ENST00000342992.11:c.96699G>T
(TTN)
|
ENSP00000343764.6:p.Lys32233Asn
|
|
ENST00000342175.11:c.77784G>T
(TTN)
|
ENSP00000340554.6:p.Lys25928Asn
|
|
ENST00000359218.10:c.77583G>T
(TTN)
|
ENSP00000352154.5:p.Lys25861Asn
|
|
ENST00000342175.10:c.77784G>T
(TTN)
|
ENSP00000340554.6:p.Lys25928Asn
|
|
ENST00000342992.10:c.96699G>T
(TTN)
|
ENSP00000343764.6:p.Lys32233Asn
|
|
ENST00000359218.9:c.77583G>T
(TTN)
|
ENSP00000352154.5:p.Lys25861Asn
|
|
ENST00000460472.6:c.77208G>T
(TTN)
|
ENSP00000434586.1:p.Lys25736Asn
|
|
ENST00000589042.5:c.104403G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys34801Asn
|
|
ENST00000591111.5:c.99480G>T
(TTN)
|
ENSP00000465570.1:p.Lys33160Asn
|
|
ENST00000615779.4:c.99480G>T
(TTN)
|
ENSP00000483597.1:p.Lys33160Asn
|
|
NM_001256850.1:c.99480G>T
(TTN)
|
NP_001243779.1:p.Lys33160Asn
|
|
NM_001267550.2:c.104403G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Lys34801Asn
|
|
NM_003319.4:c.77208G>T
(TTN)
|
NP_003310.4:p.Lys25736Asn
|
|
NM_133378.4:c.96699G>T
(TTN)
|
NP_596869.4:p.Lys32233Asn
|
|
NM_133432.3:c.77583G>T
(TTN)
|
NP_597676.3:p.Lys25861Asn
|
|
NM_133437.4:c.77784G>T
(TTN)
|
NP_597681.4:p.Lys25928Asn
|
|
NR_038271.1:n.446+8576C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3520C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.103500G>T
(TTN)
|
XP_011510031.1:p.Lys34500Asn
|
|
XM_011511730.1:c.77394G>T
(TTN)
|
XP_011510032.1:p.Lys25798Asn
|
|
XM_011511731.1:c.77253G>T
(TTN)
|
XP_011510033.1:p.Lys25751Asn
|
|
XM_017004819.1:c.103296G>T
(TTN)
|
XP_016860308.1:p.Lys34432Asn
|
|
XM_017004820.1:c.98694G>T
(TTN)
|
XP_016860309.1:p.Lys32898Asn
|
|
XM_017004821.1:c.98691G>T
(TTN)
|
XP_016860310.1:p.Lys32897Asn
|
|
XM_017004822.1:c.95733G>T
(TTN)
|
XP_016860311.1:p.Lys31911Asn
|
|
XM_017004823.1:c.77349G>T
(TTN)
|
XP_016860312.1:p.Lys25783Asn
|
|
XM_024453094.1:c.98844G>T
(TTN)
|
XP_024308862.1:p.Lys32948Asn
|
|
XM_024453095.1:c.98841G>T
(TTN)
|
XP_024308863.1:p.Lys32947Asn
|
|
XM_024453096.1:c.98274G>T
(TTN)
|
XP_024308864.1:p.Lys32758Asn
|
|
XM_024453097.1:c.95616G>T
(TTN)
|
XP_024308865.1:p.Lys31872Asn
|
|
XM_024453098.1:c.95535G>T
(TTN)
|
XP_024308866.1:p.Lys31845Asn
|
|
XM_024453099.1:c.77298G>T
(TTN)
|
XP_024308867.1:p.Lys25766Asn
|
|
XM_024453100.1:c.67152G>T
(TTN)
|
XP_024308868.1:p.Lys22384Asn
|
|