ENST00000237596.7:c.1492C>G
MANE Select
|
ENSP00000237596.2:p.His498Asp
|
|
ENST00000237596.6:c.1492C>G
|
ENSP00000237596.2:p.His498Asp
|
|
ENST00000508588.5:c.-199+3357C>G
|
ENSP00000427131.1:n.-199+3357C>G
|
|
NM_000297.3:c.1492C>G
|
NP_000288.1:p.His498Asp
|
|
XM_011532028.1:c.1267C>G
|
XP_011530330.1:p.His423Asp
|
|
XM_011532029.1:c.772C>G
|
XP_011530331.1:p.His258Asp
|
|
XM_011532030.1:c.652C>G
|
XP_011530332.1:p.His218Asp
|
|
XR_244632.2:n.1587C>G
|
|
|
NR_156488.1:n.1579C>G
|
|
|
XM_011532028.2:c.1267C>G
|
XP_011530330.1:p.His423Asp
|
|
XM_011532030.2:c.652C>G
|
XP_011530332.1:p.His218Asp
|
|
NM_000297.4:c.1492C>G
MANE Select
|
NP_000288.1:p.His498Asp
|
|
NR_156488.2:n.1591C>G
|
|
|