ENST00000342992.11:c.86984T>C
(TTN)
|
ENSP00000343764.6:p.Ile28995Thr
|
|
ENST00000342175.11:c.68069T>C
(TTN)
|
ENSP00000340554.6:p.Ile22690Thr
|
|
ENST00000359218.10:c.67868T>C
(TTN)
|
ENSP00000352154.5:p.Ile22623Thr
|
|
ENST00000342175.10:c.68069T>C
(TTN)
|
ENSP00000340554.6:p.Ile22690Thr
|
|
ENST00000342992.10:c.86984T>C
(TTN)
|
ENSP00000343764.6:p.Ile28995Thr
|
|
ENST00000359218.9:c.67868T>C
(TTN)
|
ENSP00000352154.5:p.Ile22623Thr
|
|
ENST00000460472.6:c.67493T>C
(TTN)
|
ENSP00000434586.1:p.Ile22498Thr
|
|
ENST00000589042.5:c.94688T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile31563Thr
|
|
ENST00000591111.5:c.89765T>C
(TTN)
|
ENSP00000465570.1:p.Ile29922Thr
|
|
ENST00000615779.4:c.89765T>C
(TTN)
|
ENSP00000483597.1:p.Ile29922Thr
|
|
NM_001256850.1:c.89765T>C
(TTN)
|
NP_001243779.1:p.Ile29922Thr
|
|
NM_001267550.2:c.94688T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ile31563Thr
|
|
NM_003319.4:c.67493T>C
(TTN)
|
NP_003310.4:p.Ile22498Thr
|
|
NM_133378.4:c.86984T>C
(TTN)
|
NP_596869.4:p.Ile28995Thr
|
|
NM_133432.3:c.67868T>C
(TTN)
|
NP_597676.3:p.Ile22623Thr
|
|
NM_133437.4:c.68069T>C
(TTN)
|
NP_597681.4:p.Ile22690Thr
|
|
NR_038271.1:n.446+23104A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+4379A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.93785T>C
(TTN)
|
XP_011510031.1:p.Ile31262Thr
|
|
XM_011511730.1:c.67679T>C
(TTN)
|
XP_011510032.1:p.Ile22560Thr
|
|
XM_011511731.1:c.67538T>C
(TTN)
|
XP_011510033.1:p.Ile22513Thr
|
|
XM_017004819.1:c.93581T>C
(TTN)
|
XP_016860308.1:p.Ile31194Thr
|
|
XM_017004820.1:c.88979T>C
(TTN)
|
XP_016860309.1:p.Ile29660Thr
|
|
XM_017004821.1:c.88976T>C
(TTN)
|
XP_016860310.1:p.Ile29659Thr
|
|
XM_017004822.1:c.86018T>C
(TTN)
|
XP_016860311.1:p.Ile28673Thr
|
|
XM_017004823.1:c.67634T>C
(TTN)
|
XP_016860312.1:p.Ile22545Thr
|
|
XM_024453094.1:c.89129T>C
(TTN)
|
XP_024308862.1:p.Ile29710Thr
|
|
XM_024453095.1:c.89126T>C
(TTN)
|
XP_024308863.1:p.Ile29709Thr
|
|
XM_024453096.1:c.88559T>C
(TTN)
|
XP_024308864.1:p.Ile29520Thr
|
|
XM_024453097.1:c.85901T>C
(TTN)
|
XP_024308865.1:p.Ile28634Thr
|
|
XM_024453098.1:c.85820T>C
(TTN)
|
XP_024308866.1:p.Ile28607Thr
|
|
XM_024453099.1:c.67583T>C
(TTN)
|
XP_024308867.1:p.Ile22528Thr
|
|
XM_024453100.1:c.57437T>C
(TTN)
|
XP_024308868.1:p.Ile19146Thr
|
|