ENST00000248633.9:c.951G>C
MANE Select
|
ENSP00000248633.4:p.Trp317Cys
|
|
ENST00000248633.8:c.951G>C
|
ENSP00000248633.4:p.Trp317Cys
|
|
ENST00000428214.5:c.951G>C
|
ENSP00000394413.1:p.Trp317Cys
|
|
ENST00000438045.5:c.274-3597G>C
|
ENSP00000410438.1:n.274-3597G>C
|
|
ENST00000484913.5:n.990G>C
|
|
|
NM_000466.2:c.951G>C
|
NP_000457.1:p.Trp317Cys
|
|
NM_001282677.1:c.951G>C
|
NP_001269606.1:p.Trp317Cys
|
|
NM_001282678.1:c.327G>C
|
NP_001269607.1:p.Trp109Cys
|
|
XR_242246.3:n.1047G>C
|
|
|
XM_017012319.2:c.-716G>C
|
XP_016867808.1:n.-716G>C
|
|
XR_001744808.2:n.61G>C
|
|
|
XR_242246.5:n.998G>C
|
|
|
NM_000466.3:c.951G>C
MANE Select
|
NP_000457.1:p.Trp317Cys
|
|
NM_001282677.2:c.951G>C
|
NP_001269606.1:p.Trp317Cys
|
|
NM_001282678.2:c.327G>C
|
NP_001269607.1:p.Trp109Cys
|
|