ENST00000248633.9:c.1136A>T
MANE Select
|
ENSP00000248633.4:p.Glu379Val
|
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ENST00000248633.8:c.1136A>T
|
ENSP00000248633.4:p.Glu379Val
|
|
ENST00000422866.1:c.37A>T
|
|
|
ENST00000428214.5:c.1136A>T
|
ENSP00000394413.1:p.Glu379Val
|
|
ENST00000438045.5:c.274-3412A>T
|
ENSP00000410438.1:n.274-3412A>T
|
|
ENST00000484913.5:n.1175A>T
|
|
|
NM_000466.2:c.1136A>T
|
NP_000457.1:p.Glu379Val
|
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NM_001282677.1:c.1136A>T
|
NP_001269606.1:p.Glu379Val
|
|
NM_001282678.1:c.512A>T
|
NP_001269607.1:p.Glu171Val
|
|
XR_242246.3:n.1232A>T
|
|
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XM_017012319.2:c.-531A>T
|
XP_016867808.1:n.-531A>T
|
|
XR_001744808.2:n.246A>T
|
|
|
XR_242246.5:n.1183A>T
|
|
|
NM_000466.3:c.1136A>T
MANE Select
|
NP_000457.1:p.Glu379Val
|
|
NM_001282677.2:c.1136A>T
|
NP_001269606.1:p.Glu379Val
|
|
NM_001282678.2:c.512A>T
|
NP_001269607.1:p.Glu171Val
|
|