ENST00000342992.11:c.78799T>G
(TTN)
|
ENSP00000343764.6:p.Ser26267Ala
|
|
ENST00000342175.11:c.59884T>G
(TTN)
|
ENSP00000340554.6:p.Ser19962Ala
|
|
ENST00000359218.10:c.59683T>G
(TTN)
|
ENSP00000352154.5:p.Ser19895Ala
|
|
ENST00000342175.10:c.59884T>G
(TTN)
|
ENSP00000340554.6:p.Ser19962Ala
|
|
ENST00000342992.10:c.78799T>G
(TTN)
|
ENSP00000343764.6:p.Ser26267Ala
|
|
ENST00000359218.9:c.59683T>G
(TTN)
|
ENSP00000352154.5:p.Ser19895Ala
|
|
ENST00000460472.6:c.59308T>G
(TTN)
|
ENSP00000434586.1:p.Ser19770Ala
|
|
ENST00000589042.5:c.86503T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser28835Ala
|
|
ENST00000591111.5:c.81580T>G
(TTN)
|
ENSP00000465570.1:p.Ser27194Ala
|
|
ENST00000615779.4:c.81580T>G
(TTN)
|
ENSP00000483597.1:p.Ser27194Ala
|
|
NM_001256850.1:c.81580T>G
(TTN)
|
NP_001243779.1:p.Ser27194Ala
|
|
NM_001267550.2:c.86503T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser28835Ala
|
|
NM_003319.4:c.59308T>G
(TTN)
|
NP_003310.4:p.Ser19770Ala
|
|
NM_133378.4:c.78799T>G
(TTN)
|
NP_596869.4:p.Ser26267Ala
|
|
NM_133432.3:c.59683T>G
(TTN)
|
NP_597676.3:p.Ser19895Ala
|
|
NM_133437.4:c.59884T>G
(TTN)
|
NP_597681.4:p.Ser19962Ala
|
|
NR_038271.1:n.447-11671A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17268A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.85600T>G
(TTN)
|
XP_011510031.1:p.Ser28534Ala
|
|
XM_011511730.1:c.59494T>G
(TTN)
|
XP_011510032.1:p.Ser19832Ala
|
|
XM_011511731.1:c.59353T>G
(TTN)
|
XP_011510033.1:p.Ser19785Ala
|
|
XM_017004819.1:c.85396T>G
(TTN)
|
XP_016860308.1:p.Ser28466Ala
|
|
XM_017004820.1:c.80794T>G
(TTN)
|
XP_016860309.1:p.Ser26932Ala
|
|
XM_017004821.1:c.80791T>G
(TTN)
|
XP_016860310.1:p.Ser26931Ala
|
|
XM_017004822.1:c.77833T>G
(TTN)
|
XP_016860311.1:p.Ser25945Ala
|
|
XM_017004823.1:c.59449T>G
(TTN)
|
XP_016860312.1:p.Ser19817Ala
|
|
XM_024453094.1:c.80944T>G
(TTN)
|
XP_024308862.1:p.Ser26982Ala
|
|
XM_024453095.1:c.80941T>G
(TTN)
|
XP_024308863.1:p.Ser26981Ala
|
|
XM_024453096.1:c.80374T>G
(TTN)
|
XP_024308864.1:p.Ser26792Ala
|
|
XM_024453097.1:c.77716T>G
(TTN)
|
XP_024308865.1:p.Ser25906Ala
|
|
XM_024453098.1:c.77635T>G
(TTN)
|
XP_024308866.1:p.Ser25879Ala
|
|
XM_024453099.1:c.59398T>G
(TTN)
|
XP_024308867.1:p.Ser19800Ala
|
|
XM_024453100.1:c.49252T>G
(TTN)
|
XP_024308868.1:p.Ser16418Ala
|
|