ENST00000695850.1:n.1547A>G
|
|
|
ENST00000695852.1:n.478A>G
|
|
|
ENST00000695853.1:c.*1430A>G
|
ENSP00000512218.1:n.*1430A>G
|
|
ENST00000423902.7:c.8371A>G
MANE Select
|
ENSP00000392028.1:p.Asn2791Asp
|
|
ENST00000423902.6:c.8371A>G
|
ENSP00000392028.1:p.Asn2791Asp
|
|
ENST00000524602.5:c.2224A>G
|
ENSP00000437061.1:p.Asn742Asp
|
|
ENST00000528280.1:n.417A>G
|
|
|
NM_001316690.1:c.2224A>G
|
NP_001303619.1:p.Asn742Asp
|
|
NM_017780.3:c.8371A>G
|
NP_060250.2:p.Asn2791Asp
|
|
XM_011517553.1:c.8461A>G
|
XP_011515855.1:p.Asn2821Asp
|
|
XM_011517554.1:c.8461A>G
|
XP_011515856.1:p.Asn2821Asp
|
|
XM_011517555.1:c.8458A>G
|
XP_011515857.1:p.Asn2820Asp
|
|
XM_011517556.1:c.8239A>G
|
XP_011515858.1:p.Asn2747Asp
|
|
XM_011517557.1:c.6448A>G
|
XP_011515859.1:p.Asn2150Asp
|
|
XM_011517558.1:c.5998A>G
|
XP_011515860.1:p.Asn2000Asp
|
|
XM_011517559.1:c.5206A>G
|
XP_011515861.1:p.Asn1736Asp
|
|
XM_011517553.2:c.8461A>G
|
XP_011515855.1:p.Asn2821Asp
|
|
XM_011517554.3:c.8461A>G
|
XP_011515856.1:p.Asn2821Asp
|
|
XM_011517555.2:c.8458A>G
|
XP_011515857.1:p.Asn2820Asp
|
|
XM_017013612.1:c.8461A>G
|
XP_016869101.1:p.Asn2821Asp
|
|
XM_017013613.1:c.8368A>G
|
XP_016869102.1:p.Asn2790Asp
|
|
NM_017780.4:c.8371A>G
MANE Select
|
NP_060250.2:p.Asn2791Asp
|
|