ENST00000237596.7:c.979A>T
MANE Select
|
ENSP00000237596.2:p.Arg327Ter
|
|
ENST00000237596.6:c.979A>T
|
ENSP00000237596.2:p.Arg327Ter
|
|
ENST00000506367.1:n.426A>T
|
|
|
NM_000297.3:c.979A>T
|
NP_000288.1:p.Arg327Ter
|
|
XM_011532028.1:c.979A>T
|
XP_011530330.1:p.Arg327Ter
|
|
XM_011532029.1:c.259A>T
|
XP_011530331.1:p.Arg87Ter
|
|
XM_011532030.1:c.139A>T
|
XP_011530332.1:p.Arg47Ter
|
|
XR_244632.2:n.1074A>T
|
|
|
NR_156488.1:n.1066A>T
|
|
|
XM_011532028.2:c.979A>T
|
XP_011530330.1:p.Arg327Ter
|
|
XM_011532030.2:c.139A>T
|
XP_011530332.1:p.Arg47Ter
|
|
NM_000297.4:c.979A>T
MANE Select
|
NP_000288.1:p.Arg327Ter
|
|
NR_156488.2:n.1078A>T
|
|
|