ENST00000237596.7:c.1472A>G
MANE Select
|
ENSP00000237596.2:p.Glu491Gly
|
|
ENST00000237596.6:c.1472A>G
|
ENSP00000237596.2:p.Glu491Gly
|
|
ENST00000508588.5:c.-199+3337A>G
|
ENSP00000427131.1:n.-199+3337A>G
|
|
NM_000297.3:c.1472A>G
|
NP_000288.1:p.Glu491Gly
|
|
XM_011532028.1:c.1247A>G
|
XP_011530330.1:p.Glu416Gly
|
|
XM_011532029.1:c.752A>G
|
XP_011530331.1:p.Glu251Gly
|
|
XM_011532030.1:c.632A>G
|
XP_011530332.1:p.Glu211Gly
|
|
XR_244632.2:n.1567A>G
|
|
|
NR_156488.1:n.1559A>G
|
|
|
XM_011532028.2:c.1247A>G
|
XP_011530330.1:p.Glu416Gly
|
|
XM_011532030.2:c.632A>G
|
XP_011530332.1:p.Glu211Gly
|
|
NM_000297.4:c.1472A>G
MANE Select
|
NP_000288.1:p.Glu491Gly
|
|
NR_156488.2:n.1571A>G
|
|
|