ENST00000248633.9:c.2622A>G
MANE Select
|
ENSP00000248633.4:p.Arg874=
|
|
ENST00000248633.8:c.2622A>G
|
ENSP00000248633.4:p.Arg874=
|
|
ENST00000428214.5:c.2451A>G
|
ENSP00000394413.1:p.Arg817=
|
|
ENST00000438045.5:c.1656A>G
|
ENSP00000410438.1:p.Arg552=
|
|
ENST00000484913.5:n.2661A>G
|
|
|
ENST00000496420.5:n.2514A>G
|
|
|
NM_000466.2:c.2622A>G
|
NP_000457.1:p.Arg874=
|
|
NM_001282677.1:c.2451A>G
|
NP_001269606.1:p.Arg817=
|
|
NM_001282678.1:c.1998A>G
|
NP_001269607.1:p.Arg666=
|
|
XM_005250433.3:c.873A>G
|
XP_005250490.1:p.Arg291=
|
|
XR_242246.3:n.2718A>G
|
|
|
XM_017012319.2:c.873A>G
|
XP_016867808.1:p.Arg291=
|
|
XR_001744808.2:n.1649A>G
|
|
|
XR_242246.5:n.2669A>G
|
|
|
NM_000466.3:c.2622A>G
MANE Select
|
NP_000457.1:p.Arg874=
|
|
NM_001282677.2:c.2451A>G
|
NP_001269606.1:p.Arg817=
|
|
NM_001282678.2:c.1998A>G
|
NP_001269607.1:p.Arg666=
|
|