ENST00000237596.7:c.1430A>G
MANE Select
|
ENSP00000237596.2:p.Glu477Gly
|
|
ENST00000237596.6:c.1430A>G
|
ENSP00000237596.2:p.Glu477Gly
|
|
ENST00000508588.5:c.-199+3295A>G
|
ENSP00000427131.1:n.-199+3295A>G
|
|
NM_000297.3:c.1430A>G
|
NP_000288.1:p.Glu477Gly
|
|
XM_011532028.1:c.1205A>G
|
XP_011530330.1:p.Glu402Gly
|
|
XM_011532029.1:c.710A>G
|
XP_011530331.1:p.Glu237Gly
|
|
XM_011532030.1:c.590A>G
|
XP_011530332.1:p.Glu197Gly
|
|
XR_244632.2:n.1525A>G
|
|
|
NR_156488.1:n.1517A>G
|
|
|
XM_011532028.2:c.1205A>G
|
XP_011530330.1:p.Glu402Gly
|
|
XM_011532030.2:c.590A>G
|
XP_011530332.1:p.Glu197Gly
|
|
NM_000297.4:c.1430A>G
MANE Select
|
NP_000288.1:p.Glu477Gly
|
|
NR_156488.2:n.1529A>G
|
|
|