Amino acid replacement: E387V.
A8067405T
E387V | mys-PA; E387V | mys-PB; E387V | mys-PC; E387V | mys-PD
E387V
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Weak allele.
Selected as: a mutation that permits the survival of an F1 male.