ENST00000342992.11:c.98430C>T
(TTN)
|
ENSP00000343764.6:p.Ala32810=
|
|
ENST00000342175.11:c.79515C>T
(TTN)
|
ENSP00000340554.6:p.Ala26505=
|
|
ENST00000359218.10:c.79314C>T
(TTN)
|
ENSP00000352154.5:p.Ala26438=
|
|
ENST00000342175.10:c.79515C>T
(TTN)
|
ENSP00000340554.6:p.Ala26505=
|
|
ENST00000342992.10:c.98430C>T
(TTN)
|
ENSP00000343764.6:p.Ala32810=
|
|
ENST00000359218.9:c.79314C>T
(TTN)
|
ENSP00000352154.5:p.Ala26438=
|
|
ENST00000460472.6:c.78939C>T
(TTN)
|
ENSP00000434586.1:p.Ala26313=
|
|
ENST00000589042.5:c.106134C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala35378=
|
|
ENST00000591111.5:c.101211C>T
(TTN)
|
ENSP00000465570.1:p.Ala33737=
|
|
ENST00000615779.4:c.101211C>T
(TTN)
|
ENSP00000483597.1:p.Ala33737=
|
|
NM_001256850.1:c.101211C>T
(TTN)
|
NP_001243779.1:p.Ala33737=
|
|
NM_001267550.2:c.106134C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala35378=
|
|
NM_003319.4:c.78939C>T
(TTN)
|
NP_003310.4:p.Ala26313=
|
|
NM_133378.4:c.98430C>T
(TTN)
|
NP_596869.4:p.Ala32810=
|
|
NM_133432.3:c.79314C>T
(TTN)
|
NP_597676.3:p.Ala26438=
|
|
NM_133437.4:c.79515C>T
(TTN)
|
NP_597681.4:p.Ala26505=
|
|
NR_038271.1:n.446+6845G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5251G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105231C>T
(TTN)
|
XP_011510031.1:p.Ala35077=
|
|
XM_011511730.1:c.79125C>T
(TTN)
|
XP_011510032.1:p.Ala26375=
|
|
XM_011511731.1:c.78984C>T
(TTN)
|
XP_011510033.1:p.Ala26328=
|
|
XM_017004819.1:c.105027C>T
(TTN)
|
XP_016860308.1:p.Ala35009=
|
|
XM_017004820.1:c.100425C>T
(TTN)
|
XP_016860309.1:p.Ala33475=
|
|
XM_017004821.1:c.100422C>T
(TTN)
|
XP_016860310.1:p.Ala33474=
|
|
XM_017004822.1:c.97464C>T
(TTN)
|
XP_016860311.1:p.Ala32488=
|
|
XM_017004823.1:c.79080C>T
(TTN)
|
XP_016860312.1:p.Ala26360=
|
|
XM_024453094.1:c.100575C>T
(TTN)
|
XP_024308862.1:p.Ala33525=
|
|
XM_024453095.1:c.100572C>T
(TTN)
|
XP_024308863.1:p.Ala33524=
|
|
XM_024453096.1:c.100005C>T
(TTN)
|
XP_024308864.1:p.Ala33335=
|
|
XM_024453097.1:c.97347C>T
(TTN)
|
XP_024308865.1:p.Ala32449=
|
|
XM_024453098.1:c.97266C>T
(TTN)
|
XP_024308866.1:p.Ala32422=
|
|
XM_024453099.1:c.79029C>T
(TTN)
|
XP_024308867.1:p.Ala26343=
|
|
XM_024453100.1:c.68883C>T
(TTN)
|
XP_024308868.1:p.Ala22961=
|
|