ENST00000237596.7:c.1191A>G
MANE Select
|
ENSP00000237596.2:p.Arg397=
|
|
ENST00000237596.6:c.1191A>G
|
ENSP00000237596.2:p.Arg397=
|
|
ENST00000506367.1:n.638A>G
|
|
|
ENST00000508588.5:c.-327A>G
|
ENSP00000427131.1:n.-327A>G
|
|
NM_000297.3:c.1191A>G
|
NP_000288.1:p.Arg397=
|
|
XM_011532028.1:c.1095-3313A>G
|
XP_011530330.1:n.1095-3313A>G
|
|
XM_011532029.1:c.471A>G
|
XP_011530331.1:p.Arg157=
|
|
XM_011532030.1:c.351A>G
|
XP_011530332.1:p.Arg117=
|
|
XR_244632.2:n.1286A>G
|
|
|
NR_156488.1:n.1278A>G
|
|
|
XM_011532028.2:c.1095-3313A>G
|
XP_011530330.1:n.1095-3313A>G
|
|
XM_011532030.2:c.351A>G
|
XP_011530332.1:p.Arg117=
|
|
NM_000297.4:c.1191A>G
MANE Select
|
NP_000288.1:p.Arg397=
|
|
NR_156488.2:n.1290A>G
|
|
|