ENST00000695850.1:n.1416A>G
|
|
|
ENST00000695852.1:n.347A>G
|
|
|
ENST00000695853.1:c.*1299A>G
|
ENSP00000512218.1:n.*1299A>G
|
|
ENST00000423902.7:c.8240A>G
MANE Select
|
ENSP00000392028.1:p.Asn2747Ser
|
|
ENST00000423902.6:c.8240A>G
|
ENSP00000392028.1:p.Asn2747Ser
|
|
ENST00000524602.5:c.2093A>G
|
ENSP00000437061.1:p.Asn698Ser
|
|
ENST00000528280.1:n.286A>G
|
|
|
NM_001316690.1:c.2093A>G
|
NP_001303619.1:p.Asn698Ser
|
|
NM_017780.3:c.8240A>G
|
NP_060250.2:p.Asn2747Ser
|
|
XM_011517553.1:c.8330A>G
|
XP_011515855.1:p.Asn2777Ser
|
|
XM_011517554.1:c.8330A>G
|
XP_011515856.1:p.Asn2777Ser
|
|
XM_011517555.1:c.8327A>G
|
XP_011515857.1:p.Asn2776Ser
|
|
XM_011517556.1:c.8108A>G
|
XP_011515858.1:p.Asn2703Ser
|
|
XM_011517557.1:c.6317A>G
|
XP_011515859.1:p.Asn2106Ser
|
|
XM_011517558.1:c.5867A>G
|
XP_011515860.1:p.Asn1956Ser
|
|
XM_011517559.1:c.5075A>G
|
XP_011515861.1:p.Asn1692Ser
|
|
XM_011517553.2:c.8330A>G
|
XP_011515855.1:p.Asn2777Ser
|
|
XM_011517554.3:c.8330A>G
|
XP_011515856.1:p.Asn2777Ser
|
|
XM_011517555.2:c.8327A>G
|
XP_011515857.1:p.Asn2776Ser
|
|
XM_017013612.1:c.8330A>G
|
XP_016869101.1:p.Asn2777Ser
|
|
XM_017013613.1:c.8237A>G
|
XP_016869102.1:p.Asn2746Ser
|
|
NM_017780.4:c.8240A>G
MANE Select
|
NP_060250.2:p.Asn2747Ser
|
|