ENST00000237596.7:c.1086T>G
MANE Select
|
ENSP00000237596.2:p.Asn362Lys
|
|
ENST00000237596.6:c.1086T>G
|
ENSP00000237596.2:p.Asn362Lys
|
|
ENST00000506367.1:n.533T>G
|
|
|
NM_000297.3:c.1086T>G
|
NP_000288.1:p.Asn362Lys
|
|
XM_011532028.1:c.1086T>G
|
XP_011530330.1:p.Asn362Lys
|
|
XM_011532029.1:c.366T>G
|
XP_011530331.1:p.Asn122Lys
|
|
XM_011532030.1:c.246T>G
|
XP_011530332.1:p.Asn82Lys
|
|
XR_244632.2:n.1181T>G
|
|
|
NR_156488.1:n.1173T>G
|
|
|
XM_011532028.2:c.1086T>G
|
XP_011530330.1:p.Asn362Lys
|
|
XM_011532030.2:c.246T>G
|
XP_011530332.1:p.Asn82Lys
|
|
NM_000297.4:c.1086T>G
MANE Select
|
NP_000288.1:p.Asn362Lys
|
|
NR_156488.2:n.1185T>G
|
|
|