ENST00000696156.1:c.490G=
|
ENSP00000512446.1:p.Asp164=
|
|
ENST00000696157.1:c.*791G=
|
ENSP00000512447.1:n.*791G=
|
|
ENST00000696158.1:c.*828G=
|
ENSP00000512448.1:n.*828G=
|
|
ENST00000696159.1:c.*497G=
|
ENSP00000512449.1:n.*497G=
|
|
ENST00000696160.1:c.601G=
|
ENSP00000512450.1:p.Asp201=
|
|
ENST00000696161.1:c.704G=
|
ENSP00000512451.1:p.Arg235=
|
|
ENST00000696162.1:c.*1293G=
|
ENSP00000512452.1:n.*1293G=
|
|
ENST00000696163.1:c.523G=
|
ENSP00000512453.1:p.Asp175=
|
|
ENST00000261623.8:c.574G=
MANE Select
|
ENSP00000261623.3:p.Asp192=
|
|
ENST00000261623.7:c.574G=
|
ENSP00000261623.3:p.Asp192=
|
|
NM_000101.3:c.574G=
|
NP_000092.2:p.Asp192=
|
|
NM_000101.4:c.574G=
MANE Select
|
NP_000092.2:p.Asp192=
|
|