ENST00000683572.1:n.748C>G
|
|
|
ENST00000341947.7:c.4942C>G
MANE Select
|
ENSP00000339915.2:p.His1648Asp
|
|
ENST00000341947.6:c.4942C>G
|
ENSP00000339915.2:p.His1648Asp
|
|
ENST00000361917.5:c.4621C>G
|
ENSP00000355123.1:p.His1541Asp
|
|
ENST00000374708.8:c.4684C>G
|
ENSP00000363840.4:p.His1562Asp
|
|
ENST00000477772.1:n.732C>G
|
|
|
NM_080679.2:c.4621C>G
|
NP_542410.2:p.His1541Asp
|
|
NM_080680.2:c.4942C>G
|
NP_542411.2:p.His1648Asp
|
|
NM_080681.2:c.4684C>G
|
NP_542412.2:p.His1562Asp
|
|
XM_011514298.1:c.4096C>G
|
XP_011512600.1:p.His1366Asp
|
|
XM_011514299.1:c.4228C>G
|
XP_011512601.1:p.His1410Asp
|
|
XM_011514300.1:c.4048C>G
|
XP_011512602.1:p.His1350Asp
|
|
XM_011514301.1:c.3985C>G
|
XP_011512603.1:p.His1329Asp
|
|
XM_011514302.1:c.3829C>G
|
XP_011512604.1:p.His1277Asp
|
|
XM_011514299.2:c.4228C>G
|
XP_011512601.1:p.His1410Asp
|
|
XM_011514300.2:c.4048C>G
|
XP_011512602.1:p.His1350Asp
|
|
XM_011514302.2:c.3829C>G
|
XP_011512604.1:p.His1277Asp
|
|
XM_017010250.1:c.4942C>G
|
XP_016865739.1:p.His1648Asp
|
|
XM_017010251.2:c.3760C>G
|
XP_016865740.1:p.His1254Asp
|
|
NM_080680.3:c.4942C>G
MANE Select
|
NP_542411.2:p.His1648Asp
|
|
NM_080681.3:c.4684C>G
|
NP_542412.2:p.His1562Asp
|
|
NM_080679.3:c.4621C>G
|
NP_542410.2:p.His1541Asp
|
|