ENST00000378823.8:c.3193G>C
MANE Select
|
ENSP00000368100.4:p.Asp1065His
|
|
ENST00000638452.2:c.2896G>C
|
ENSP00000492349.2:p.Asp966His
|
|
ENST00000638504.1:n.2801G>C
|
|
|
ENST00000638568.2:c.2896G>C
|
ENSP00000491158.2:p.Asp966His
|
|
ENST00000639899.1:n.3712G>C
|
|
|
ENST00000640655.2:c.2896G>C
|
ENSP00000491596.2:p.Asp966His
|
|
ENST00000651249.1:c.29G>C
|
|
|
ENST00000378823.7:c.3193G>C
|
ENSP00000368100.4:p.Asp1065His
|
|
ENST00000533482.5:c.*2819G>C
|
ENSP00000431225.1:n.*2819G>C
|
|
NM_005732.3:c.3193G>C
|
NP_005723.2:p.Asp1065His
|
|
NM_005732.4:c.3193G>C
MANE Select
|
NP_005723.2:p.Asp1065His
|
|