ENST00000289473.11:c.1055A>T
MANE Select
|
ENSP00000289473.4:p.Glu352Val
|
|
ENST00000289473.10:c.1055A>T
|
ENSP00000289473.4:p.Glu352Val
|
|
ENST00000289473.8:c.1055A>T
|
ENSP00000289473.4:p.Glu352Val
|
|
ENST00000398421.6:n.2082A>T
|
|
|
ENST00000455062.2:n.1164A>T
|
|
|
NM_000265.5:c.1055A>T
|
NP_000256.4:p.Glu352Val
|
|
XM_005250543.3:c.1017A>T
|
XP_005250600.2:p.Gly339=
|
|
XM_011516498.1:c.1054A>T
|
XP_011514800.1:p.Arg352Trp
|
|
XM_011516501.1:c.662A>T
|
XP_011514803.1:p.Glu221Val
|
|
NM_000265.6:c.1055A>T
|
NP_000256.4:p.Glu352Val
|
|
NM_000265.7:c.1055A>T
MANE Select
|
NP_000256.4:p.Glu352Val
|
|