|
NM_001080.3:c.1280A>G
MANE Select
|
NP_001071.1:p.Asn427Ser
|
|
ENST00000357578.8:c.1280A>G
MANE Select
|
ENSP00000350191.3:p.Asn427Ser
|
|
NM_001368954.1:c.1136A>G
|
NP_001355883.1:p.Asn379Ser
|
|
NM_170740.1:c.1319A>G
|
NP_733936.1:p.Asn440Ser
|
|
ENST00000348925.2:c.1319A>G
|
ENSP00000314649.3:p.Asn440Ser
|
|
ENST00000357578.7:c.1280A>G
|
ENSP00000350191.3:p.Asn427Ser
|
|
ENST00000479394.1:n.395A>G
|
|
|
ENST00000479394.2:n.395A>G
|
|
|
ENST00000491546.5:c.1196A>G
|
ENSP00000417687.1:p.Asn399Ser
|
|
ENST00000672352.1:c.899A>G
|
ENSP00000500876.1:p.Asn300Ser
|
|
ENST00000672652.1:c.1243A>G
|
|