ENST00000237596.7:c.1081C>G
MANE Select
|
ENSP00000237596.2:p.Arg361Gly
|
|
ENST00000237596.6:c.1081C>G
|
ENSP00000237596.2:p.Arg361Gly
|
|
ENST00000506367.1:n.528C>G
|
|
|
NM_000297.3:c.1081C>G
|
NP_000288.1:p.Arg361Gly
|
|
XM_011532028.1:c.1081C>G
|
XP_011530330.1:p.Arg361Gly
|
|
XM_011532029.1:c.361C>G
|
XP_011530331.1:p.Arg121Gly
|
|
XM_011532030.1:c.241C>G
|
XP_011530332.1:p.Arg81Gly
|
|
XR_244632.2:n.1176C>G
|
|
|
NR_156488.1:n.1168C>G
|
|
|
XM_011532028.2:c.1081C>G
|
XP_011530330.1:p.Arg361Gly
|
|
XM_011532030.2:c.241C>G
|
XP_011530332.1:p.Arg81Gly
|
|
NM_000297.4:c.1081C>G
MANE Select
|
NP_000288.1:p.Arg361Gly
|
|
NR_156488.2:n.1180C>G
|
|
|