ENST00000248633.9:c.2221A>C
MANE Select
|
ENSP00000248633.4:p.Asn741His
|
|
ENST00000248633.8:c.2221A>C
|
ENSP00000248633.4:p.Asn741His
|
|
ENST00000428214.5:c.2050A>C
|
ENSP00000394413.1:p.Asn684His
|
|
ENST00000438045.5:c.1255A>C
|
ENSP00000410438.1:p.Asn419His
|
|
ENST00000484913.5:n.2260A>C
|
|
|
ENST00000496092.1:n.19A>C
|
|
|
ENST00000496420.5:n.1897A>C
|
|
|
NM_000466.2:c.2221A>C
|
NP_000457.1:p.Asn741His
|
|
NM_001282677.1:c.2050A>C
|
NP_001269606.1:p.Asn684His
|
|
NM_001282678.1:c.1597A>C
|
NP_001269607.1:p.Asn533His
|
|
XM_005250433.3:c.472A>C
|
XP_005250490.1:p.Asn158His
|
|
XR_242246.3:n.2317A>C
|
|
|
XM_017012319.2:c.472A>C
|
XP_016867808.1:p.Asn158His
|
|
XR_001744808.2:n.1248A>C
|
|
|
XR_242246.5:n.2268A>C
|
|
|
NM_000466.3:c.2221A>C
MANE Select
|
NP_000457.1:p.Asn741His
|
|
NM_001282677.2:c.2050A>C
|
NP_001269606.1:p.Asn684His
|
|
NM_001282678.2:c.1597A>C
|
NP_001269607.1:p.Asn533His
|
|