ENST00000342992.11:c.72164A>C
(TTN)
|
ENSP00000343764.6:p.Glu24055Ala
|
|
ENST00000342175.11:c.53249A>C
(TTN)
|
ENSP00000340554.6:p.Glu17750Ala
|
|
ENST00000359218.10:c.53048A>C
(TTN)
|
ENSP00000352154.5:p.Glu17683Ala
|
|
ENST00000342175.10:c.53249A>C
(TTN)
|
ENSP00000340554.6:p.Glu17750Ala
|
|
ENST00000342992.10:c.72164A>C
(TTN)
|
ENSP00000343764.6:p.Glu24055Ala
|
|
ENST00000359218.9:c.53048A>C
(TTN)
|
ENSP00000352154.5:p.Glu17683Ala
|
|
ENST00000460472.6:c.52673A>C
(TTN)
|
ENSP00000434586.1:p.Glu17558Ala
|
|
ENST00000589042.5:c.79868A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu26623Ala
|
|
ENST00000591111.5:c.74945A>C
(TTN)
|
ENSP00000465570.1:p.Glu24982Ala
|
|
ENST00000615779.4:c.74945A>C
(TTN)
|
ENSP00000483597.1:p.Glu24982Ala
|
|
NM_001256850.1:c.74945A>C
(TTN)
|
NP_001243779.1:p.Glu24982Ala
|
|
NM_001267550.2:c.79868A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu26623Ala
|
|
NM_003319.4:c.52673A>C
(TTN)
|
NP_003310.4:p.Glu17558Ala
|
|
NM_133378.4:c.72164A>C
(TTN)
|
NP_596869.4:p.Glu24055Ala
|
|
NM_133432.3:c.53048A>C
(TTN)
|
NP_597676.3:p.Glu17683Ala
|
|
NM_133437.4:c.53249A>C
(TTN)
|
NP_597681.4:p.Glu17750Ala
|
|
NR_038271.1:n.447-5036T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-16308T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.78965A>C
(TTN)
|
XP_011510031.1:p.Glu26322Ala
|
|
XM_011511730.1:c.52859A>C
(TTN)
|
XP_011510032.1:p.Glu17620Ala
|
|
XM_011511731.1:c.52718A>C
(TTN)
|
XP_011510033.1:p.Glu17573Ala
|
|
XM_017004819.1:c.78761A>C
(TTN)
|
XP_016860308.1:p.Glu26254Ala
|
|
XM_017004820.1:c.74159A>C
(TTN)
|
XP_016860309.1:p.Glu24720Ala
|
|
XM_017004821.1:c.74156A>C
(TTN)
|
XP_016860310.1:p.Glu24719Ala
|
|
XM_017004822.1:c.71198A>C
(TTN)
|
XP_016860311.1:p.Glu23733Ala
|
|
XM_017004823.1:c.52814A>C
(TTN)
|
XP_016860312.1:p.Glu17605Ala
|
|
XM_024453094.1:c.74309A>C
(TTN)
|
XP_024308862.1:p.Glu24770Ala
|
|
XM_024453095.1:c.74306A>C
(TTN)
|
XP_024308863.1:p.Glu24769Ala
|
|
XM_024453096.1:c.73739A>C
(TTN)
|
XP_024308864.1:p.Glu24580Ala
|
|
XM_024453097.1:c.71081A>C
(TTN)
|
XP_024308865.1:p.Glu23694Ala
|
|
XM_024453098.1:c.71000A>C
(TTN)
|
XP_024308866.1:p.Glu23667Ala
|
|
XM_024453099.1:c.52763A>C
(TTN)
|
XP_024308867.1:p.Glu17588Ala
|
|
XM_024453100.1:c.42617A>C
(TTN)
|
XP_024308868.1:p.Glu14206Ala
|
|