ENST00000237596.7:c.1510A>G
MANE Select
|
ENSP00000237596.2:p.Arg504Gly
|
|
ENST00000237596.6:c.1510A>G
|
ENSP00000237596.2:p.Arg504Gly
|
|
ENST00000508588.5:c.-199+3375A>G
|
ENSP00000427131.1:n.-199+3375A>G
|
|
NM_000297.3:c.1510A>G
|
NP_000288.1:p.Arg504Gly
|
|
XM_011532028.1:c.1285A>G
|
XP_011530330.1:p.Arg429Gly
|
|
XM_011532029.1:c.790A>G
|
XP_011530331.1:p.Arg264Gly
|
|
XM_011532030.1:c.670A>G
|
XP_011530332.1:p.Arg224Gly
|
|
XR_244632.2:n.1605A>G
|
|
|
NR_156488.1:n.1597A>G
|
|
|
XM_011532028.2:c.1285A>G
|
XP_011530330.1:p.Arg429Gly
|
|
XM_011532030.2:c.670A>G
|
XP_011530332.1:p.Arg224Gly
|
|
NM_000297.4:c.1510A>G
MANE Select
|
NP_000288.1:p.Arg504Gly
|
|
NR_156488.2:n.1609A>G
|
|
|