ENST00000342992.11:c.100208T>A
(TTN)
|
ENSP00000343764.6:p.Leu33403Gln
|
|
ENST00000342175.11:c.81293T>A
(TTN)
|
ENSP00000340554.6:p.Leu27098Gln
|
|
ENST00000359218.10:c.81092T>A
(TTN)
|
ENSP00000352154.5:p.Leu27031Gln
|
|
ENST00000342175.10:c.81293T>A
(TTN)
|
ENSP00000340554.6:p.Leu27098Gln
|
|
ENST00000342992.10:c.100208T>A
(TTN)
|
ENSP00000343764.6:p.Leu33403Gln
|
|
ENST00000359218.9:c.81092T>A
(TTN)
|
ENSP00000352154.5:p.Leu27031Gln
|
|
ENST00000460472.6:c.80717T>A
(TTN)
|
ENSP00000434586.1:p.Leu26906Gln
|
|
ENST00000589042.5:c.107912T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35971Gln
|
|
ENST00000591111.5:c.102989T>A
(TTN)
|
ENSP00000465570.1:p.Leu34330Gln
|
|
ENST00000615779.4:c.102989T>A
(TTN)
|
ENSP00000483597.1:p.Leu34330Gln
|
|
NM_001256850.1:c.102989T>A
(TTN)
|
NP_001243779.1:p.Leu34330Gln
|
|
NM_001267550.2:c.107912T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35971Gln
|
|
NM_003319.4:c.80717T>A
(TTN)
|
NP_003310.4:p.Leu26906Gln
|
|
NM_133378.4:c.100208T>A
(TTN)
|
NP_596869.4:p.Leu33403Gln
|
|
NM_133432.3:c.81092T>A
(TTN)
|
NP_597676.3:p.Leu27031Gln
|
|
NM_133437.4:c.81293T>A
(TTN)
|
NP_597681.4:p.Leu27098Gln
|
|
NR_038271.1:n.446+3440A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3440A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.107009T>A
(TTN)
|
XP_011510031.1:p.Leu35670Gln
|
|
XM_011511730.1:c.80903T>A
(TTN)
|
XP_011510032.1:p.Leu26968Gln
|
|
XM_011511731.1:c.80762T>A
(TTN)
|
XP_011510033.1:p.Leu26921Gln
|
|
XM_017004819.1:c.106805T>A
(TTN)
|
XP_016860308.1:p.Leu35602Gln
|
|
XM_017004820.1:c.102203T>A
(TTN)
|
XP_016860309.1:p.Leu34068Gln
|
|
XM_017004821.1:c.102200T>A
(TTN)
|
XP_016860310.1:p.Leu34067Gln
|
|
XM_017004822.1:c.99242T>A
(TTN)
|
XP_016860311.1:p.Leu33081Gln
|
|
XM_017004823.1:c.80858T>A
(TTN)
|
XP_016860312.1:p.Leu26953Gln
|
|
XM_024453094.1:c.102353T>A
(TTN)
|
XP_024308862.1:p.Leu34118Gln
|
|
XM_024453095.1:c.102350T>A
(TTN)
|
XP_024308863.1:p.Leu34117Gln
|
|
XM_024453096.1:c.101783T>A
(TTN)
|
XP_024308864.1:p.Leu33928Gln
|
|
XM_024453097.1:c.99125T>A
(TTN)
|
XP_024308865.1:p.Leu33042Gln
|
|
XM_024453098.1:c.99044T>A
(TTN)
|
XP_024308866.1:p.Leu33015Gln
|
|
XM_024453099.1:c.80807T>A
(TTN)
|
XP_024308867.1:p.Leu26936Gln
|
|
XM_024453100.1:c.70661T>A
(TTN)
|
XP_024308868.1:p.Leu23554Gln
|
|