ENST00000248633.9:c.2005G>C
MANE Select
|
ENSP00000248633.4:p.Gly669Arg
|
|
ENST00000248633.8:c.2005G>C
|
ENSP00000248633.4:p.Gly669Arg
|
|
ENST00000428214.5:c.1900+1450G>C
|
ENSP00000394413.1:n.1900+1450G>C
|
|
ENST00000438045.5:c.1039G>C
|
ENSP00000410438.1:p.Gly347Arg
|
|
ENST00000484913.5:n.2044G>C
|
|
|
ENST00000496420.5:n.1681G>C
|
|
|
NM_000466.2:c.2005G>C
|
NP_000457.1:p.Gly669Arg
|
|
NM_001282677.1:c.1900+1450G>C
|
NP_001269606.1:n.1900+1450G>C
|
|
NM_001282678.1:c.1381G>C
|
NP_001269607.1:p.Gly461Arg
|
|
XM_005250433.3:c.256G>C
|
XP_005250490.1:p.Gly86Arg
|
|
XR_242246.3:n.2101G>C
|
|
|
XM_017012319.2:c.256G>C
|
XP_016867808.1:p.Gly86Arg
|
|
XR_001744808.2:n.1032G>C
|
|
|
XR_242246.5:n.2052G>C
|
|
|
NM_000466.3:c.2005G>C
MANE Select
|
NP_000457.1:p.Gly669Arg
|
|
NM_001282677.2:c.1900+1450G>C
|
NP_001269606.1:n.1900+1450G>C
|
|
NM_001282678.2:c.1381G>C
|
NP_001269607.1:p.Gly461Arg
|
|