ENST00000647956.2:c.1086C>A
MANE Select
|
ENSP00000497341.1:p.Gly362=
|
|
ENST00000648162.1:n.1058C>A
|
|
|
ENST00000649804.1:c.180C>A
|
ENSP00000497938.1:p.Gly60=
|
|
ENST00000535233.6:c.984C>A
|
ENSP00000438636.3:p.Gly328=
|
|
ENST00000536053.6:c.1128C>A
|
ENSP00000444271.3:p.Gly376=
|
|
ENST00000540394.5:n.2151C>A
|
|
|
ENST00000542285.5:c.1086C>A
|
ENSP00000438615.2:p.Gly362=
|
|
ENST00000602298.2:n.1435C>A
|
|
|
NM_001733.4:c.1086C>A
|
NP_001724.3:p.Gly362=
|
|
NM_001354346.1:c.1128C>A
|
NP_001341275.1:p.Gly376=
|
|
NM_001733.6:c.1086C>A
|
NP_001724.4:p.Gly362=
|
|
NM_001733.7:c.1086C>A
MANE Select
|
NP_001724.4:p.Gly362=
|
|
NM_001354346.2:c.1128C>A
|
NP_001341275.1:p.Gly376=
|
|