ENST00000248633.9:c.2278G>C
MANE Select
|
ENSP00000248633.4:p.Asp760His
|
|
ENST00000248633.8:c.2278G>C
|
ENSP00000248633.4:p.Asp760His
|
|
ENST00000428214.5:c.2107G>C
|
ENSP00000394413.1:p.Asp703His
|
|
ENST00000438045.5:c.1312G>C
|
ENSP00000410438.1:p.Asp438His
|
|
ENST00000484913.5:n.2317G>C
|
|
|
ENST00000496092.1:n.76G>C
|
|
|
ENST00000496420.5:n.1954G>C
|
|
|
NM_000466.2:c.2278G>C
|
NP_000457.1:p.Asp760His
|
|
NM_001282677.1:c.2107G>C
|
NP_001269606.1:p.Asp703His
|
|
NM_001282678.1:c.1654G>C
|
NP_001269607.1:p.Asp552His
|
|
XM_005250433.3:c.529G>C
|
XP_005250490.1:p.Asp177His
|
|
XR_242246.3:n.2374G>C
|
|
|
XM_017012319.2:c.529G>C
|
XP_016867808.1:p.Asp177His
|
|
XR_001744808.2:n.1305G>C
|
|
|
XR_242246.5:n.2325G>C
|
|
|
NM_000466.3:c.2278G>C
MANE Select
|
NP_000457.1:p.Asp760His
|
|
NM_001282677.2:c.2107G>C
|
NP_001269606.1:p.Asp703His
|
|
NM_001282678.2:c.1654G>C
|
NP_001269607.1:p.Asp552His
|
|