ENST00000456935.7:c.1527C>T
MANE Select
|
ENSP00000395473.2:p.Arg509=
|
|
ENST00000221363.8:c.1524C>T
|
ENSP00000221363.4:p.Arg508=
|
|
ENST00000433513.5:n.133C>T
|
|
|
ENST00000456935.6:c.1527C>T
|
ENSP00000395473.2:p.Arg509=
|
|
ENST00000466794.5:n.1426C>T
|
|
|
ENST00000495617.1:n.703C>T
|
|
|
ENST00000593686.1:c.137C>T
|
|
|
ENST00000595880.5:n.124C>T
|
|
|
NM_000528.3:c.1527C>T
|
NP_000519.2:p.Arg509=
|
|
NM_001173498.1:c.1524C>T
|
NP_001166969.1:p.Arg508=
|
|
XM_005259913.1:c.1530C>T
|
XP_005259970.1:p.Arg510=
|
|
XM_011528017.1:c.426C>T
|
XP_011526319.1:p.Arg142=
|
|
XM_005259913.2:c.1530C>T
|
XP_005259970.1:p.Arg510=
|
|
XM_024451518.1:c.426C>T
|
XP_024307286.1:p.Arg142=
|
|
NM_000528.4:c.1527C>T
MANE Select
|
NP_000519.2:p.Arg509=
|
|
NM_001173498.2:c.1524C>T
|
NP_001166969.1:p.Arg508=
|
|