ENST00000342992.11:c.88350T>G
(TTN)
|
ENSP00000343764.6:p.Asp29450Glu
|
|
ENST00000342175.11:c.69435T>G
(TTN)
|
ENSP00000340554.6:p.Asp23145Glu
|
|
ENST00000359218.10:c.69234T>G
(TTN)
|
ENSP00000352154.5:p.Asp23078Glu
|
|
ENST00000342175.10:c.69435T>G
(TTN)
|
ENSP00000340554.6:p.Asp23145Glu
|
|
ENST00000342992.10:c.88350T>G
(TTN)
|
ENSP00000343764.6:p.Asp29450Glu
|
|
ENST00000359218.9:c.69234T>G
(TTN)
|
ENSP00000352154.5:p.Asp23078Glu
|
|
ENST00000460472.6:c.68859T>G
(TTN)
|
ENSP00000434586.1:p.Asp22953Glu
|
|
ENST00000589042.5:c.96054T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp32018Glu
|
|
ENST00000591111.5:c.91131T>G
(TTN)
|
ENSP00000465570.1:p.Asp30377Glu
|
|
ENST00000615779.4:c.91131T>G
(TTN)
|
ENSP00000483597.1:p.Asp30377Glu
|
|
NM_001256850.1:c.91131T>G
(TTN)
|
NP_001243779.1:p.Asp30377Glu
|
|
NM_001267550.2:c.96054T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp32018Glu
|
|
NM_003319.4:c.68859T>G
(TTN)
|
NP_003310.4:p.Asp22953Glu
|
|
NM_133378.4:c.88350T>G
(TTN)
|
NP_596869.4:p.Asp29450Glu
|
|
NM_133432.3:c.69234T>G
(TTN)
|
NP_597676.3:p.Asp23078Glu
|
|
NM_133437.4:c.69435T>G
(TTN)
|
NP_597681.4:p.Asp23145Glu
|
|
NR_038271.1:n.446+20454A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1729A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.95151T>G
(TTN)
|
XP_011510031.1:p.Asp31717Glu
|
|
XM_011511730.1:c.69045T>G
(TTN)
|
XP_011510032.1:p.Asp23015Glu
|
|
XM_011511731.1:c.68904T>G
(TTN)
|
XP_011510033.1:p.Asp22968Glu
|
|
XM_017004819.1:c.94947T>G
(TTN)
|
XP_016860308.1:p.Asp31649Glu
|
|
XM_017004820.1:c.90345T>G
(TTN)
|
XP_016860309.1:p.Asp30115Glu
|
|
XM_017004821.1:c.90342T>G
(TTN)
|
XP_016860310.1:p.Asp30114Glu
|
|
XM_017004822.1:c.87384T>G
(TTN)
|
XP_016860311.1:p.Asp29128Glu
|
|
XM_017004823.1:c.69000T>G
(TTN)
|
XP_016860312.1:p.Asp23000Glu
|
|
XM_024453094.1:c.90495T>G
(TTN)
|
XP_024308862.1:p.Asp30165Glu
|
|
XM_024453095.1:c.90492T>G
(TTN)
|
XP_024308863.1:p.Asp30164Glu
|
|
XM_024453096.1:c.89925T>G
(TTN)
|
XP_024308864.1:p.Asp29975Glu
|
|
XM_024453097.1:c.87267T>G
(TTN)
|
XP_024308865.1:p.Asp29089Glu
|
|
XM_024453098.1:c.87186T>G
(TTN)
|
XP_024308866.1:p.Asp29062Glu
|
|
XM_024453099.1:c.68949T>G
(TTN)
|
XP_024308867.1:p.Asp22983Glu
|
|
XM_024453100.1:c.58803T>G
(TTN)
|
XP_024308868.1:p.Asp19601Glu
|
|