ENST00000334529.10:c.802A>G
MANE Select
|
ENSP00000333919.5:p.Asn268Asp
|
|
ENST00000334529.9:c.802A>G
|
ENSP00000333919.5:p.Asn268Asp
|
|
ENST00000383680.4:c.658A>G
|
ENSP00000373178.4:p.Asn220Asp
|
|
ENST00000474965.1:n.306A>G
|
|
|
NM_001085357.1:c.658A>G
|
NP_001078826.1:p.Asn220Asp
|
|
NM_181780.3:c.802A>G
|
NP_861445.3:p.Asn268Asp
|
|
XM_011512446.1:c.820A>G
|
XP_011510748.1:p.Asn274Asp
|
|
XM_011512447.1:c.820A>G
|
XP_011510749.1:p.Asn274Asp
|
|
XM_011512447.3:c.820A>G
|
XP_011510749.1:p.Asn274Asp
|
|
XM_017005748.2:c.802A>G
|
XP_016861237.1:p.Asn268Asp
|
|
NM_181780.4:c.802A>G
MANE Select
|
NP_861445.4:p.Asn268Asp
|
|
NM_001085357.2:c.658A>G
|
NP_001078826.1:p.Asn220Asp
|
|