Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_001079668.3
p.P299L
c.896C>T
Surrounding Variants
NM_001079668.3
p.G297_P299delFs
c.890_896del7
NM_001079668.3
p.K298I
c.893A>T
NM_001079668.3
p.G297S
c.889G>A
NM_001079668.3
p.A302V
c.905C>T
NM_003317.4
p.K265delFs
c.793delT
NM_003317.4
p.G273delFs
c.818delC
NM_001079668.3
p.V294G
c.881T>G
NM_001079668.3
p.L293del1
c.877_878delCAG
NM_003317.4
p.L263fs
c.787_788fs
NM_001079668.3
p.L293insFs
c.877dupC
NM_001079668.3
p.L293Q
c.878T>A
NM_003317.4
p.V262_L263delFs
c.786_787delGG
NM_001079668.3
p.V292_L293delFs
c.876_877delGG