ENST00000378823.8:c.2398A>G
MANE Select
|
ENSP00000368100.4:p.Met800Val
|
|
ENST00000638452.2:c.2101A>G
|
ENSP00000492349.2:p.Met701Val
|
|
ENST00000638504.1:n.2006A>G
|
|
|
ENST00000638568.2:c.2101A>G
|
ENSP00000491158.2:p.Met701Val
|
|
ENST00000639899.1:n.2917A>G
|
|
|
ENST00000640655.2:c.2101A>G
|
ENSP00000491596.2:p.Met701Val
|
|
ENST00000651160.1:c.*542A>G
|
ENSP00000498829.1:n.*542A>G
|
|
ENST00000651658.1:n.2941A>G
|
|
|
ENST00000651723.1:c.*2481A>G
|
ENSP00000498237.1:n.*2481A>G
|
|
ENST00000652016.1:c.*615A>G
|
ENSP00000498267.1:n.*615A>G
|
|
ENST00000652485.1:c.2431A>G
|
ENSP00000498973.1:p.Met811Val
|
|
ENST00000378823.7:c.2398A>G
|
ENSP00000368100.4:p.Met800Val
|
|
ENST00000423956.5:c.*584A>G
|
ENSP00000390971.1:n.*584A>G
|
|
ENST00000533482.5:c.*2024A>G
|
ENSP00000431225.1:n.*2024A>G
|
|
NM_005732.3:c.2398A>G
|
NP_005723.2:p.Met800Val
|
|
NM_005732.4:c.2398A>G
MANE Select
|
NP_005723.2:p.Met800Val
|
|