Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001001669.3
p.L165P
c.494T>C
Surrounding Variants
NM_001001669.3
p.P154L
c.461C>T
NM_001001669.3
p.Q180*
c.538C>T
NM_001001669.3
p.Q197delFs
c.589_590delCA
NM_001001669.3
p.Q197fs
c.589_590fs
NM_001001669.3
p.V206M
c.616G>A
NM_001001669.3
p.N207D
c.619A>G
NM_001001669.3
p.V219V
c.657G>A
NM_001001669.3
p.E227E
c.681G>A
NM_001001669.3
p.R232Q
c.695G>A
NM_001001669.3
p.R234Q
c.701G>A
NM_001001669.3
p.A236V
c.707C>T
NM_001001669.3
p.A258S
c.772G>T