ENST00000237596.7:c.1084A>C
MANE Select
|
ENSP00000237596.2:p.Asn362His
|
|
ENST00000237596.6:c.1084A>C
|
ENSP00000237596.2:p.Asn362His
|
|
ENST00000506367.1:n.531A>C
|
|
|
NM_000297.3:c.1084A>C
|
NP_000288.1:p.Asn362His
|
|
XM_011532028.1:c.1084A>C
|
XP_011530330.1:p.Asn362His
|
|
XM_011532029.1:c.364A>C
|
XP_011530331.1:p.Asn122His
|
|
XM_011532030.1:c.244A>C
|
XP_011530332.1:p.Asn82His
|
|
XR_244632.2:n.1179A>C
|
|
|
NR_156488.1:n.1171A>C
|
|
|
XM_011532028.2:c.1084A>C
|
XP_011530330.1:p.Asn362His
|
|
XM_011532030.2:c.244A>C
|
XP_011530332.1:p.Asn82His
|
|
NM_000297.4:c.1084A>C
MANE Select
|
NP_000288.1:p.Asn362His
|
|
NR_156488.2:n.1183A>C
|
|
|