ENST00000378823.8:c.2024A>T
MANE Select
|
ENSP00000368100.4:p.Asp675Val
|
|
ENST00000638452.2:c.1727A>T
|
ENSP00000492349.2:p.Asp576Val
|
|
ENST00000638504.1:n.1632A>T
|
|
|
ENST00000638568.2:c.1727A>T
|
ENSP00000491158.2:p.Asp576Val
|
|
ENST00000639899.1:n.2543A>T
|
|
|
ENST00000640655.2:c.1727A>T
|
ENSP00000491596.2:p.Asp576Val
|
|
ENST00000651160.1:c.*168A>T
|
ENSP00000498829.1:n.*168A>T
|
|
ENST00000651658.1:n.2567A>T
|
|
|
ENST00000651723.1:c.*2107A>T
|
ENSP00000498237.1:n.*2107A>T
|
|
ENST00000652016.1:c.*241A>T
|
ENSP00000498267.1:n.*241A>T
|
|
ENST00000652485.1:c.2057A>T
|
ENSP00000498973.1:p.Asp686Val
|
|
ENST00000378823.7:c.2024A>T
|
ENSP00000368100.4:p.Asp675Val
|
|
ENST00000423956.5:c.*210A>T
|
ENSP00000390971.1:n.*210A>T
|
|
ENST00000453394.5:c.1841A>T
|
ENSP00000400049.1:p.Asp614Val
|
|
ENST00000496204.1:n.107A>T
|
|
|
ENST00000533482.5:c.*1650A>T
|
ENSP00000431225.1:n.*1650A>T
|
|
NM_005732.3:c.2024A>T
|
NP_005723.2:p.Asp675Val
|
|
NM_005732.4:c.2024A>T
MANE Select
|
NP_005723.2:p.Asp675Val
|
|