ENST00000361066.7:c.581C>T
(GSTM3)
MANE Select
|
ENSP00000354357.2:p.Ala194Val
|
|
ENST00000256594.7:c.581C>T
(GSTM3)
|
ENSP00000256594.3:p.Ala194Val
|
|
ENST00000361066.6:c.581C>T
(GSTM3)
|
ENSP00000354357.2:p.Ala194Val
|
|
ENST00000429410.2:n.82+24820G>A
(GSTM5)
|
|
|
ENST00000476321.5:n.549C>T
(GSTM3)
|
|
|
ENST00000486823.5:n.545C>T
(GSTM3)
|
|
|
ENST00000488824.1:n.926C>T
(GSTM3)
|
|
|
NM_000849.4:c.581C>T
(GSTM3)
|
NP_000840.2:p.Ala194Val
|
|
NR_024537.1:n.815C>T
(GSTM3)
|
|
|
XM_011541296.1:c.800C>T
(GSTM3)
|
XP_011539598.1:p.Ala267Val
|
|
NM_000849.5:c.581C>T
(GSTM3)
MANE Select
|
NP_000840.2:p.Ala194Val
|
|
NR_024537.2:n.815C>T
(GSTM3)
|
|
|