ENST00000248633.9:c.1133A>T
MANE Select
|
ENSP00000248633.4:p.Asp378Val
|
|
ENST00000248633.8:c.1133A>T
|
ENSP00000248633.4:p.Asp378Val
|
|
ENST00000422866.1:c.34A>T
|
|
|
ENST00000428214.5:c.1133A>T
|
ENSP00000394413.1:p.Asp378Val
|
|
ENST00000438045.5:c.274-3415A>T
|
ENSP00000410438.1:n.274-3415A>T
|
|
ENST00000484913.5:n.1172A>T
|
|
|
NM_000466.2:c.1133A>T
|
NP_000457.1:p.Asp378Val
|
|
NM_001282677.1:c.1133A>T
|
NP_001269606.1:p.Asp378Val
|
|
NM_001282678.1:c.509A>T
|
NP_001269607.1:p.Asp170Val
|
|
XR_242246.3:n.1229A>T
|
|
|
XM_017012319.2:c.-534A>T
|
XP_016867808.1:n.-534A>T
|
|
XR_001744808.2:n.243A>T
|
|
|
XR_242246.5:n.1180A>T
|
|
|
NM_000466.3:c.1133A>T
MANE Select
|
NP_000457.1:p.Asp378Val
|
|
NM_001282677.2:c.1133A>T
|
NP_001269606.1:p.Asp378Val
|
|
NM_001282678.2:c.509A>T
|
NP_001269607.1:p.Asp170Val
|
|