ENST00000456935.7:c.1461A>G
MANE Select
|
ENSP00000395473.2:p.Lys487=
|
|
ENST00000221363.8:c.1458A>G
|
ENSP00000221363.4:p.Lys486=
|
|
ENST00000433513.5:n.67A>G
|
|
|
ENST00000456935.6:c.1461A>G
|
ENSP00000395473.2:p.Lys487=
|
|
ENST00000466794.5:n.1360A>G
|
|
|
ENST00000495617.1:n.637A>G
|
|
|
ENST00000593686.1:c.71A>G
|
|
|
ENST00000595880.5:n.58A>G
|
|
|
NM_000528.3:c.1461A>G
|
NP_000519.2:p.Lys487=
|
|
NM_001173498.1:c.1458A>G
|
NP_001166969.1:p.Lys486=
|
|
XM_005259913.1:c.1464A>G
|
XP_005259970.1:p.Lys488=
|
|
XM_011528017.1:c.360A>G
|
XP_011526319.1:p.Lys120=
|
|
XM_005259913.2:c.1464A>G
|
XP_005259970.1:p.Lys488=
|
|
XM_024451518.1:c.360A>G
|
XP_024307286.1:p.Lys120=
|
|
NM_000528.4:c.1461A>G
MANE Select
|
NP_000519.2:p.Lys487=
|
|
NM_001173498.2:c.1458A>G
|
NP_001166969.1:p.Lys486=
|
|