ENST00000248633.9:c.2179G>C
MANE Select
|
ENSP00000248633.4:p.Gly727Arg
|
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ENST00000248633.8:c.2179G>C
|
ENSP00000248633.4:p.Gly727Arg
|
|
ENST00000428214.5:c.2008G>C
|
ENSP00000394413.1:p.Gly670Arg
|
|
ENST00000438045.5:c.1213G>C
|
ENSP00000410438.1:p.Gly405Arg
|
|
ENST00000484913.5:n.2218G>C
|
|
|
ENST00000496420.5:n.1855G>C
|
|
|
NM_000466.2:c.2179G>C
|
NP_000457.1:p.Gly727Arg
|
|
NM_001282677.1:c.2008G>C
|
NP_001269606.1:p.Gly670Arg
|
|
NM_001282678.1:c.1555G>C
|
NP_001269607.1:p.Gly519Arg
|
|
XM_005250433.3:c.430G>C
|
XP_005250490.1:p.Gly144Arg
|
|
XR_242246.3:n.2275G>C
|
|
|
XM_017012319.2:c.430G>C
|
XP_016867808.1:p.Gly144Arg
|
|
XR_001744808.2:n.1206G>C
|
|
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XR_242246.5:n.2226G>C
|
|
|
NM_000466.3:c.2179G>C
MANE Select
|
NP_000457.1:p.Gly727Arg
|
|
NM_001282677.2:c.2008G>C
|
NP_001269606.1:p.Gly670Arg
|
|
NM_001282678.2:c.1555G>C
|
NP_001269607.1:p.Gly519Arg
|
|