ENST00000547400.6:c.589G>C
|
ENSP00000446724.2:p.Asp197His
|
|
ENST00000551576.6:c.859G>C
|
ENSP00000455848.2:p.Asp287His
|
|
ENST00000552678.2:c.859G>C
|
ENSP00000457394.2:p.Asp287His
|
|
ENST00000388922.9:c.859G>C
MANE Select
|
ENSP00000373574.4:p.Asp287His
|
|
ENST00000388922.8:c.859G>C
|
ENSP00000373574.4:p.Asp287His
|
|
ENST00000419526.6:c.337G>C
|
ENSP00000392492.2:p.Asp113His
|
|
ENST00000550683.5:c.901G>C
|
ENSP00000447884.1:p.Asp301His
|
|
NM_000020.2:c.859G>C , LRG_543t1:c.859G>C
|
NP_000011.2:p.Asp287His
|
|
NM_001077401.1:c.859G>C
|
NP_001070869.1:p.Asp287His
|
|
XM_005269235.2:c.859G>C
|
XP_005269292.1:p.Asp287His
|
|
XM_011539008.1:c.589G>C
|
XP_011537310.1:p.Asp197His
|
|
XM_024449279.1:c.70G>C
|
XP_024305047.1:p.Asp24His
|
|
NM_000020.3:c.859G>C
MANE Select
|
NP_000011.2:p.Asp287His
|
|
NM_001077401.2:c.859G>C
|
NP_001070869.1:p.Asp287His
|
|