ENST00000647956.2:c.1041G=
MANE Select
|
ENSP00000497341.1:p.Gly347=
|
|
ENST00000648162.1:n.1013G=
|
|
|
ENST00000649804.1:c.135G=
|
ENSP00000497938.1:p.Gly45=
|
|
ENST00000535233.6:c.939G=
|
ENSP00000438636.3:p.Gly313=
|
|
ENST00000536053.6:c.1083G=
|
ENSP00000444271.3:p.Gly361=
|
|
ENST00000540394.5:n.2106G=
|
|
|
ENST00000542285.5:c.1041G=
|
ENSP00000438615.2:p.Gly347=
|
|
ENST00000602298.2:n.1390G=
|
|
|
NM_001733.4:c.1041G=
|
NP_001724.3:p.Gly347=
|
|
NM_001354346.1:c.1083G=
|
NP_001341275.1:p.Gly361=
|
|
NM_001733.6:c.1041G=
|
NP_001724.4:p.Gly347=
|
|
NM_001733.7:c.1041G=
MANE Select
|
NP_001724.4:p.Gly347=
|
|
NM_001354346.2:c.1083G=
|
NP_001341275.1:p.Gly361=
|
|