ENST00000342992.11:c.52907T>C
(TTN)
|
ENSP00000343764.6:p.Val17636Ala
|
|
ENST00000342175.11:c.33992T>C
(TTN)
|
ENSP00000340554.6:p.Val11331Ala
|
|
ENST00000359218.10:c.33791T>C
(TTN)
|
ENSP00000352154.5:p.Val11264Ala
|
|
ENST00000342175.10:c.33992T>C
(TTN)
|
ENSP00000340554.6:p.Val11331Ala
|
|
ENST00000342992.10:c.52907T>C
(TTN)
|
ENSP00000343764.6:p.Val17636Ala
|
|
ENST00000359218.9:c.33791T>C
(TTN)
|
ENSP00000352154.5:p.Val11264Ala
|
|
ENST00000460472.6:c.33416T>C
(TTN)
|
ENSP00000434586.1:p.Val11139Ala
|
|
ENST00000589042.5:c.60611T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val20204Ala
|
|
ENST00000591111.5:c.55688T>C
(TTN)
|
ENSP00000465570.1:p.Val18563Ala
|
|
ENST00000615779.4:c.55688T>C
(TTN)
|
ENSP00000483597.1:p.Val18563Ala
|
|
NM_001256850.1:c.55688T>C
(TTN)
|
NP_001243779.1:p.Val18563Ala
|
|
NM_001267550.2:c.60611T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val20204Ala
|
|
NM_003319.4:c.33416T>C
(TTN)
|
NP_003310.4:p.Val11139Ala
|
|
NM_133378.4:c.52907T>C
(TTN)
|
NP_596869.4:p.Val17636Ala
|
|
NM_133432.3:c.33791T>C
(TTN)
|
NP_597676.3:p.Val11264Ala
|
|
NM_133437.4:c.33992T>C
(TTN)
|
NP_597681.4:p.Val11331Ala
|
|
NR_038271.1:n.597-6482A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-25A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.59708T>C
(TTN)
|
XP_011510031.1:p.Val19903Ala
|
|
XM_011511730.1:c.33602T>C
(TTN)
|
XP_011510032.1:p.Val11201Ala
|
|
XM_011511731.1:c.33461T>C
(TTN)
|
XP_011510033.1:p.Val11154Ala
|
|
XM_017004819.1:c.59504T>C
(TTN)
|
XP_016860308.1:p.Val19835Ala
|
|
XM_017004820.1:c.54902T>C
(TTN)
|
XP_016860309.1:p.Val18301Ala
|
|
XM_017004821.1:c.54899T>C
(TTN)
|
XP_016860310.1:p.Val18300Ala
|
|
XM_017004822.1:c.51941T>C
(TTN)
|
XP_016860311.1:p.Val17314Ala
|
|
XM_017004823.1:c.33557T>C
(TTN)
|
XP_016860312.1:p.Val11186Ala
|
|
XM_024453094.1:c.55052T>C
(TTN)
|
XP_024308862.1:p.Val18351Ala
|
|
XM_024453095.1:c.55049T>C
(TTN)
|
XP_024308863.1:p.Val18350Ala
|
|
XM_024453096.1:c.54482T>C
(TTN)
|
XP_024308864.1:p.Val18161Ala
|
|
XM_024453097.1:c.51824T>C
(TTN)
|
XP_024308865.1:p.Val17275Ala
|
|
XM_024453098.1:c.51743T>C
(TTN)
|
XP_024308866.1:p.Val17248Ala
|
|
XM_024453099.1:c.33506T>C
(TTN)
|
XP_024308867.1:p.Val11169Ala
|
|
XM_024453100.1:c.23360T>C
(TTN)
|
XP_024308868.1:p.Val7787Ala
|
|