ENST00000342992.11:c.68543A>C
(TTN)
|
ENSP00000343764.6:p.Asp22848Ala
|
|
ENST00000342175.11:c.49628A>C
(TTN)
|
ENSP00000340554.6:p.Asp16543Ala
|
|
ENST00000359218.10:c.49427A>C
(TTN)
|
ENSP00000352154.5:p.Asp16476Ala
|
|
ENST00000342175.10:c.49628A>C
(TTN)
|
ENSP00000340554.6:p.Asp16543Ala
|
|
ENST00000342992.10:c.68543A>C
(TTN)
|
ENSP00000343764.6:p.Asp22848Ala
|
|
ENST00000359218.9:c.49427A>C
(TTN)
|
ENSP00000352154.5:p.Asp16476Ala
|
|
ENST00000460472.6:c.49052A>C
(TTN)
|
ENSP00000434586.1:p.Asp16351Ala
|
|
ENST00000589042.5:c.76247A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp25416Ala
|
|
ENST00000591111.5:c.71324A>C
(TTN)
|
ENSP00000465570.1:p.Asp23775Ala
|
|
ENST00000615779.4:c.71324A>C
(TTN)
|
ENSP00000483597.1:p.Asp23775Ala
|
|
NM_001256850.1:c.71324A>C
(TTN)
|
NP_001243779.1:p.Asp23775Ala
|
|
NM_001267550.2:c.76247A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp25416Ala
|
|
NM_003319.4:c.49052A>C
(TTN)
|
NP_003310.4:p.Asp16351Ala
|
|
NM_133378.4:c.68543A>C
(TTN)
|
NP_596869.4:p.Asp22848Ala
|
|
NM_133432.3:c.49427A>C
(TTN)
|
NP_597676.3:p.Asp16476Ala
|
|
NM_133437.4:c.49628A>C
(TTN)
|
NP_597681.4:p.Asp16543Ala
|
|
NR_038271.1:n.447-1415T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12687T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.75344A>C
(TTN)
|
XP_011510031.1:p.Asp25115Ala
|
|
XM_011511730.1:c.49238A>C
(TTN)
|
XP_011510032.1:p.Asp16413Ala
|
|
XM_011511731.1:c.49097A>C
(TTN)
|
XP_011510033.1:p.Asp16366Ala
|
|
XM_017004819.1:c.75140A>C
(TTN)
|
XP_016860308.1:p.Asp25047Ala
|
|
XM_017004820.1:c.70538A>C
(TTN)
|
XP_016860309.1:p.Asp23513Ala
|
|
XM_017004821.1:c.70535A>C
(TTN)
|
XP_016860310.1:p.Asp23512Ala
|
|
XM_017004822.1:c.67577A>C
(TTN)
|
XP_016860311.1:p.Asp22526Ala
|
|
XM_017004823.1:c.49193A>C
(TTN)
|
XP_016860312.1:p.Asp16398Ala
|
|
XM_024453094.1:c.70688A>C
(TTN)
|
XP_024308862.1:p.Asp23563Ala
|
|
XM_024453095.1:c.70685A>C
(TTN)
|
XP_024308863.1:p.Asp23562Ala
|
|
XM_024453096.1:c.70118A>C
(TTN)
|
XP_024308864.1:p.Asp23373Ala
|
|
XM_024453097.1:c.67460A>C
(TTN)
|
XP_024308865.1:p.Asp22487Ala
|
|
XM_024453098.1:c.67379A>C
(TTN)
|
XP_024308866.1:p.Asp22460Ala
|
|
XM_024453099.1:c.49142A>C
(TTN)
|
XP_024308867.1:p.Asp16381Ala
|
|
XM_024453100.1:c.38996A>C
(TTN)
|
XP_024308868.1:p.Asp12999Ala
|
|