|
NM_020751.3:c.1180A>G
MANE Select
|
NP_065802.1:p.Asn394Asp
|
|
ENST00000455146.8:c.1180A>G
MANE Select
|
ENSP00000397441.2:p.Asn394Asp
|
|
NM_001145079.1:c.1180A>G
|
NP_001138551.1:p.Asn394Asp
|
|
NM_001145079.2:c.1180A>G
|
NP_001138551.1:p.Asn394Asp
|
|
NM_020751.2:c.1180A>G
|
NP_065802.1:p.Asn394Asp
|
|
NR_026745.1:n.1345A>G
|
|
|
ENST00000356576.8:c.*1017A>G
|
ENSP00000348983.4:n.*1017A>G
|
|
ENST00000416691.5:c.1180A>G
|
ENSP00000403733.1:p.Asn394Asp
|
|
ENST00000455146.7:c.1180A>G
|
ENSP00000397441.2:p.Asn394Asp
|
|
XM_011535168.1:c.1180A>G
|
XP_011533470.1:p.Asn394Asp
|
|
XM_011535169.1:c.1024A>G
|
XP_011533471.1:p.Asn342Asp
|
|
XM_011535170.1:c.1024A>G
|
XP_011533472.1:p.Asn342Asp
|