ENST00000456935.7:c.1446G>T
MANE Select
|
ENSP00000395473.2:p.Arg482=
|
|
ENST00000221363.8:c.1443G>T
|
ENSP00000221363.4:p.Arg481=
|
|
ENST00000433513.5:n.52G>T
|
|
|
ENST00000456935.6:c.1446G>T
|
ENSP00000395473.2:p.Arg482=
|
|
ENST00000466794.5:n.1345G>T
|
|
|
ENST00000495617.1:n.622G>T
|
|
|
ENST00000593686.1:c.56G>T
|
|
|
ENST00000595880.5:n.43G>T
|
|
|
NM_000528.3:c.1446G>T
|
NP_000519.2:p.Arg482=
|
|
NM_001173498.1:c.1443G>T
|
NP_001166969.1:p.Arg481=
|
|
XM_005259913.1:c.1449G>T
|
XP_005259970.1:p.Arg483=
|
|
XM_011528017.1:c.345G>T
|
XP_011526319.1:p.Arg115=
|
|
XM_005259913.2:c.1449G>T
|
XP_005259970.1:p.Arg483=
|
|
XM_024451518.1:c.345G>T
|
XP_024307286.1:p.Arg115=
|
|
NM_000528.4:c.1446G>T
MANE Select
|
NP_000519.2:p.Arg482=
|
|
NM_001173498.2:c.1443G>T
|
NP_001166969.1:p.Arg481=
|
|