ENST00000001146.7:c.1259C>G
MANE Select
|
ENSP00000001146.2:p.Ala420Gly
|
|
ENST00000001146.6:c.1259C>G
|
ENSP00000001146.2:p.Ala420Gly
|
|
ENST00000412253.1:c.686C>G
|
ENSP00000401465.1:p.Ala229Gly
|
|
ENST00000546307.5:c.1034C>G
|
ENSP00000443304.1:p.Ala345Gly
|
|
NM_001277742.1:c.1034C>G
|
NP_001264671.1:p.Ala345Gly
|
|
NM_019885.3:c.1259C>G
|
NP_063938.1:p.Ala420Gly
|
|
XM_005264433.3:c.1085C>G
|
XP_005264490.1:p.Ala362Gly
|
|
XM_011532988.1:c.686C>G
|
XP_011531290.1:p.Ala229Gly
|
|
XM_005264433.4:c.1085C>G
|
XP_005264490.1:p.Ala362Gly
|
|
NM_001277742.2:c.1034C>G
|
NP_001264671.1:p.Ala345Gly
|
|
NM_019885.4:c.1259C>G
MANE Select
|
NP_063938.1:p.Ala420Gly
|
|