ENST00000342992.11:c.96795G>C
(TTN)
|
ENSP00000343764.6:p.Ala32265=
|
|
ENST00000342175.11:c.77880G>C
(TTN)
|
ENSP00000340554.6:p.Ala25960=
|
|
ENST00000359218.10:c.77679G>C
(TTN)
|
ENSP00000352154.5:p.Ala25893=
|
|
ENST00000342175.10:c.77880G>C
(TTN)
|
ENSP00000340554.6:p.Ala25960=
|
|
ENST00000342992.10:c.96795G>C
(TTN)
|
ENSP00000343764.6:p.Ala32265=
|
|
ENST00000359218.9:c.77679G>C
(TTN)
|
ENSP00000352154.5:p.Ala25893=
|
|
ENST00000460472.6:c.77304G>C
(TTN)
|
ENSP00000434586.1:p.Ala25768=
|
|
ENST00000589042.5:c.104499G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala34833=
|
|
ENST00000591111.5:c.99576G>C
(TTN)
|
ENSP00000465570.1:p.Ala33192=
|
|
ENST00000615779.4:c.99576G>C
(TTN)
|
ENSP00000483597.1:p.Ala33192=
|
|
NM_001256850.1:c.99576G>C
(TTN)
|
NP_001243779.1:p.Ala33192=
|
|
NM_001267550.2:c.104499G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ala34833=
|
|
NM_003319.4:c.77304G>C
(TTN)
|
NP_003310.4:p.Ala25768=
|
|
NM_133378.4:c.96795G>C
(TTN)
|
NP_596869.4:p.Ala32265=
|
|
NM_133432.3:c.77679G>C
(TTN)
|
NP_597676.3:p.Ala25893=
|
|
NM_133437.4:c.77880G>C
(TTN)
|
NP_597681.4:p.Ala25960=
|
|
NR_038271.1:n.446+8480C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3616C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103596G>C
(TTN)
|
XP_011510031.1:p.Ala34532=
|
|
XM_011511730.1:c.77490G>C
(TTN)
|
XP_011510032.1:p.Ala25830=
|
|
XM_011511731.1:c.77349G>C
(TTN)
|
XP_011510033.1:p.Ala25783=
|
|
XM_017004819.1:c.103392G>C
(TTN)
|
XP_016860308.1:p.Ala34464=
|
|
XM_017004820.1:c.98790G>C
(TTN)
|
XP_016860309.1:p.Ala32930=
|
|
XM_017004821.1:c.98787G>C
(TTN)
|
XP_016860310.1:p.Ala32929=
|
|
XM_017004822.1:c.95829G>C
(TTN)
|
XP_016860311.1:p.Ala31943=
|
|
XM_017004823.1:c.77445G>C
(TTN)
|
XP_016860312.1:p.Ala25815=
|
|
XM_024453094.1:c.98940G>C
(TTN)
|
XP_024308862.1:p.Ala32980=
|
|
XM_024453095.1:c.98937G>C
(TTN)
|
XP_024308863.1:p.Ala32979=
|
|
XM_024453096.1:c.98370G>C
(TTN)
|
XP_024308864.1:p.Ala32790=
|
|
XM_024453097.1:c.95712G>C
(TTN)
|
XP_024308865.1:p.Ala31904=
|
|
XM_024453098.1:c.95631G>C
(TTN)
|
XP_024308866.1:p.Ala31877=
|
|
XM_024453099.1:c.77394G>C
(TTN)
|
XP_024308867.1:p.Ala25798=
|
|
XM_024453100.1:c.67248G>C
(TTN)
|
XP_024308868.1:p.Ala22416=
|
|