ENST00000237596.7:c.852A>C
MANE Select
|
ENSP00000237596.2:p.Glu284Asp
|
|
ENST00000237596.6:c.852A>C
|
ENSP00000237596.2:p.Glu284Asp
|
|
ENST00000506367.1:n.299A>C
|
|
|
ENST00000506727.1:n.438A>C
|
|
|
NM_000297.3:c.852A>C
|
NP_000288.1:p.Glu284Asp
|
|
XM_011532028.1:c.852A>C
|
XP_011530330.1:p.Glu284Asp
|
|
XM_011532029.1:c.132A>C
|
XP_011530331.1:p.Glu44Asp
|
|
XM_011532030.1:c.12A>C
|
XP_011530332.1:p.Glu4Asp
|
|
XR_244632.2:n.947A>C
|
|
|
NR_156488.1:n.939A>C
|
|
|
XM_011532028.2:c.852A>C
|
XP_011530330.1:p.Glu284Asp
|
|
XM_011532030.2:c.12A>C
|
XP_011530332.1:p.Glu4Asp
|
|
NM_000297.4:c.852A>C
MANE Select
|
NP_000288.1:p.Glu284Asp
|
|
NR_156488.2:n.951A>C
|
|
|