ENST00000456935.7:c.1452A>G
MANE Select
|
ENSP00000395473.2:p.Arg484=
|
|
ENST00000221363.8:c.1449A>G
|
ENSP00000221363.4:p.Arg483=
|
|
ENST00000433513.5:n.58A>G
|
|
|
ENST00000456935.6:c.1452A>G
|
ENSP00000395473.2:p.Arg484=
|
|
ENST00000466794.5:n.1351A>G
|
|
|
ENST00000495617.1:n.628A>G
|
|
|
ENST00000593686.1:c.62A>G
|
|
|
ENST00000595880.5:n.49A>G
|
|
|
NM_000528.3:c.1452A>G
|
NP_000519.2:p.Arg484=
|
|
NM_001173498.1:c.1449A>G
|
NP_001166969.1:p.Arg483=
|
|
XM_005259913.1:c.1455A>G
|
XP_005259970.1:p.Arg485=
|
|
XM_011528017.1:c.351A>G
|
XP_011526319.1:p.Arg117=
|
|
XM_005259913.2:c.1455A>G
|
XP_005259970.1:p.Arg485=
|
|
XM_024451518.1:c.351A>G
|
XP_024307286.1:p.Arg117=
|
|
NM_000528.4:c.1452A>G
MANE Select
|
NP_000519.2:p.Arg484=
|
|
NM_001173498.2:c.1449A>G
|
NP_001166969.1:p.Arg483=
|
|