ENST00000237596.7:c.1222A>G
MANE Select
|
ENSP00000237596.2:p.Ser408Gly
|
|
ENST00000237596.6:c.1222A>G
|
ENSP00000237596.2:p.Ser408Gly
|
|
ENST00000506367.1:n.669A>G
|
|
|
ENST00000508588.5:c.-296A>G
|
ENSP00000427131.1:n.-296A>G
|
|
NM_000297.3:c.1222A>G
|
NP_000288.1:p.Ser408Gly
|
|
XM_011532028.1:c.1095-3282A>G
|
XP_011530330.1:n.1095-3282A>G
|
|
XM_011532029.1:c.502A>G
|
XP_011530331.1:p.Ser168Gly
|
|
XM_011532030.1:c.382A>G
|
XP_011530332.1:p.Ser128Gly
|
|
XR_244632.2:n.1317A>G
|
|
|
NR_156488.1:n.1309A>G
|
|
|
XM_011532028.2:c.1095-3282A>G
|
XP_011530330.1:n.1095-3282A>G
|
|
XM_011532030.2:c.382A>G
|
XP_011530332.1:p.Ser128Gly
|
|
NM_000297.4:c.1222A>G
MANE Select
|
NP_000288.1:p.Ser408Gly
|
|
NR_156488.2:n.1321A>G
|
|
|