ENST00000696156.1:c.429G=
|
ENSP00000512446.1:p.Glu143=
|
|
ENST00000696157.1:c.*730G=
|
ENSP00000512447.1:n.*730G=
|
|
ENST00000696158.1:c.*767G=
|
ENSP00000512448.1:n.*767G=
|
|
ENST00000696159.1:c.*436G=
|
ENSP00000512449.1:n.*436G=
|
|
ENST00000696160.1:c.540G=
|
ENSP00000512450.1:p.Glu180=
|
|
ENST00000696161.1:c.643G=
|
ENSP00000512451.1:p.Gly215=
|
|
ENST00000696162.1:c.*1232G=
|
ENSP00000512452.1:n.*1232G=
|
|
ENST00000696163.1:c.462G=
|
ENSP00000512453.1:p.Glu154=
|
|
ENST00000261623.8:c.513G=
MANE Select
|
ENSP00000261623.3:p.Glu171=
|
|
ENST00000261623.7:c.513G=
|
ENSP00000261623.3:p.Glu171=
|
|
NM_000101.3:c.513G=
|
NP_000092.2:p.Glu171=
|
|
NM_000101.4:c.513G=
MANE Select
|
NP_000092.2:p.Glu171=
|
|