ENST00000342992.11:c.98704G>C
(TTN)
|
ENSP00000343764.6:p.Glu32902Gln
|
|
ENST00000342175.11:c.79789G>C
(TTN)
|
ENSP00000340554.6:p.Glu26597Gln
|
|
ENST00000359218.10:c.79588G>C
(TTN)
|
ENSP00000352154.5:p.Glu26530Gln
|
|
ENST00000342175.10:c.79789G>C
(TTN)
|
ENSP00000340554.6:p.Glu26597Gln
|
|
ENST00000342992.10:c.98704G>C
(TTN)
|
ENSP00000343764.6:p.Glu32902Gln
|
|
ENST00000359218.9:c.79588G>C
(TTN)
|
ENSP00000352154.5:p.Glu26530Gln
|
|
ENST00000460472.6:c.79213G>C
(TTN)
|
ENSP00000434586.1:p.Glu26405Gln
|
|
ENST00000589042.5:c.106408G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35470Gln
|
|
ENST00000591111.5:c.101485G>C
(TTN)
|
ENSP00000465570.1:p.Glu33829Gln
|
|
ENST00000615779.4:c.101485G>C
(TTN)
|
ENSP00000483597.1:p.Glu33829Gln
|
|
NM_001256850.1:c.101485G>C
(TTN)
|
NP_001243779.1:p.Glu33829Gln
|
|
NM_001267550.2:c.106408G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35470Gln
|
|
NM_003319.4:c.79213G>C
(TTN)
|
NP_003310.4:p.Glu26405Gln
|
|
NM_133378.4:c.98704G>C
(TTN)
|
NP_596869.4:p.Glu32902Gln
|
|
NM_133432.3:c.79588G>C
(TTN)
|
NP_597676.3:p.Glu26530Gln
|
|
NM_133437.4:c.79789G>C
(TTN)
|
NP_597681.4:p.Glu26597Gln
|
|
NR_038271.1:n.446+6447C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5649C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105505G>C
(TTN)
|
XP_011510031.1:p.Glu35169Gln
|
|
XM_011511730.1:c.79399G>C
(TTN)
|
XP_011510032.1:p.Glu26467Gln
|
|
XM_011511731.1:c.79258G>C
(TTN)
|
XP_011510033.1:p.Glu26420Gln
|
|
XM_017004819.1:c.105301G>C
(TTN)
|
XP_016860308.1:p.Glu35101Gln
|
|
XM_017004820.1:c.100699G>C
(TTN)
|
XP_016860309.1:p.Glu33567Gln
|
|
XM_017004821.1:c.100696G>C
(TTN)
|
XP_016860310.1:p.Glu33566Gln
|
|
XM_017004822.1:c.97738G>C
(TTN)
|
XP_016860311.1:p.Glu32580Gln
|
|
XM_017004823.1:c.79354G>C
(TTN)
|
XP_016860312.1:p.Glu26452Gln
|
|
XM_024453094.1:c.100849G>C
(TTN)
|
XP_024308862.1:p.Glu33617Gln
|
|
XM_024453095.1:c.100846G>C
(TTN)
|
XP_024308863.1:p.Glu33616Gln
|
|
XM_024453096.1:c.100279G>C
(TTN)
|
XP_024308864.1:p.Glu33427Gln
|
|
XM_024453097.1:c.97621G>C
(TTN)
|
XP_024308865.1:p.Glu32541Gln
|
|
XM_024453098.1:c.97540G>C
(TTN)
|
XP_024308866.1:p.Glu32514Gln
|
|
XM_024453099.1:c.79303G>C
(TTN)
|
XP_024308867.1:p.Glu26435Gln
|
|
XM_024453100.1:c.69157G>C
(TTN)
|
XP_024308868.1:p.Glu23053Gln
|
|