ENST00000248633.9:c.1207A>C
MANE Select
|
ENSP00000248633.4:p.Asn403His
|
|
ENST00000248633.8:c.1207A>C
|
ENSP00000248633.4:p.Asn403His
|
|
ENST00000422866.1:c.108A>C
|
|
|
ENST00000428214.5:c.1207A>C
|
ENSP00000394413.1:p.Asn403His
|
|
ENST00000438045.5:c.274-3341A>C
|
ENSP00000410438.1:n.274-3341A>C
|
|
ENST00000484913.5:n.1246A>C
|
|
|
NM_000466.2:c.1207A>C
|
NP_000457.1:p.Asn403His
|
|
NM_001282677.1:c.1207A>C
|
NP_001269606.1:p.Asn403His
|
|
NM_001282678.1:c.583A>C
|
NP_001269607.1:p.Asn195His
|
|
XR_242246.3:n.1303A>C
|
|
|
XM_017012319.2:c.-460A>C
|
XP_016867808.1:n.-460A>C
|
|
XR_001744808.2:n.317A>C
|
|
|
XR_242246.5:n.1254A>C
|
|
|
NM_000466.3:c.1207A>C
MANE Select
|
NP_000457.1:p.Asn403His
|
|
NM_001282677.2:c.1207A>C
|
NP_001269606.1:p.Asn403His
|
|
NM_001282678.2:c.583A>C
|
NP_001269607.1:p.Asn195His
|
|