ENST00000289473.11:c.1060C>A
MANE Select
|
ENSP00000289473.4:p.Arg354=
|
|
ENST00000289473.10:c.1060C>A
|
ENSP00000289473.4:p.Arg354=
|
|
ENST00000289473.8:c.1060C>A
|
ENSP00000289473.4:p.Arg354=
|
|
ENST00000398421.6:n.2087C>A
|
|
|
ENST00000455062.2:n.1169C>A
|
|
|
NM_000265.5:c.1060C>A
|
NP_000256.4:p.Arg354=
|
|
XM_005250543.3:c.1022C>A
|
XP_005250600.2:p.Ala341Glu
|
|
XM_011516498.1:c.1059C>A
|
XP_011514800.1:p.Ser353Arg
|
|
XM_011516501.1:c.667C>A
|
XP_011514803.1:p.Arg223=
|
|
NM_000265.6:c.1060C>A
|
NP_000256.4:p.Arg354=
|
|
NM_000265.7:c.1060C>A
MANE Select
|
NP_000256.4:p.Arg354=
|
|