|
NM_001372.4:c.12047A>G
MANE Select
|
NP_001363.2:p.Asn4016Ser
|
|
ENST00000262442.9:c.12047A>G
MANE Select
|
ENSP00000262442.3:p.Asn4016Ser
|
|
NM_001372.3:c.12047A>G
|
NP_001363.2:p.Asn4016Ser
|
|
NM_004662.2:c.983A>G
|
NP_004653.2:p.Asn328Ser
|
|
ENST00000262442.8:c.12047A>G
|
ENSP00000262442.3:p.Asn4016Ser
|
|
ENST00000396001.6:n.1510A>G
|
|
|
ENST00000454412.6:c.11878-1979A>G
|
ENSP00000414874.2:n.11878-1979A>G
|
|
ENST00000608377.5:c.983A>G
|
ENSP00000476951.1:p.Asn328Ser
|
|
XM_011523703.1:c.12047A>G
|
XP_011522005.1:p.Asn4016Ser
|
|
XM_011523703.2:c.12047A>G
|
XP_011522005.1:p.Asn4016Ser
|
|
XM_017024292.2:c.11930A>G
|
XP_016879781.1:p.Asn3977Ser
|
|
XM_017024293.1:c.9929A>G
|
XP_016879782.1:p.Asn3310Ser
|