ENST00000355112.8:c.984T>C
MANE Select
|
ENSP00000347232.3:p.Ser328=
|
|
ENST00000648453.1:c.984T>C
|
ENSP00000497646.1:p.Ser328=
|
|
ENST00000680772.1:c.984T>C
|
ENSP00000506117.1:p.Ser328=
|
|
ENST00000681142.1:c.984T>C
|
ENSP00000506682.1:p.Ser328=
|
|
ENST00000355112.7:c.984T>C
|
ENSP00000347232.3:p.Ser328=
|
|
ENST00000558599.1:n.245T>C
|
|
|
ENST00000559724.5:c.984T>C
|
ENSP00000453359.1:p.Ser328=
|
|
ENST00000560509.5:c.984T>C
|
ENSP00000454158.1:p.Ser328=
|
|
NM_000057.3:c.984T>C
|
NP_000048.1:p.Ser328=
|
|
NM_001287246.1:c.984T>C
|
NP_001274175.1:p.Ser328=
|
|
NM_001287247.1:c.984T>C
|
NP_001274176.1:p.Ser328=
|
|
NM_001287248.1:c.-308T>C
|
NP_001274177.1:n.-308T>C
|
|
XM_011521881.1:c.-198T>C
|
XP_011520183.1:n.-198T>C
|
|
XM_011521882.1:c.984T>C
|
XP_011520184.1:p.Ser328=
|
|
XM_011521881.2:c.-198T>C
|
XP_011520183.1:n.-198T>C
|
|
XM_011521882.3:c.984T>C
|
XP_011520184.1:p.Ser328=
|
|
NM_000057.4:c.984T>C
MANE Select
|
NP_000048.1:p.Ser328=
|
|
NM_001287246.2:c.984T>C
|
NP_001274175.1:p.Ser328=
|
|
NM_001287247.2:c.984T>C
|
NP_001274176.1:p.Ser328=
|
|
NM_001287248.2:c.-308T>C
|
NP_001274177.1:n.-308T>C
|
|