ENST00000526189.3:c.554G>A
|
ENSP00000488104.2:p.Arg185His
|
|
ENST00000533357.5:c.635G>A
MANE Select
|
ENSP00000432943.1:p.Arg212His
|
|
ENST00000672287.2:c.47G>A
|
ENSP00000499818.2:p.Arg16His
|
|
ENST00000672602.2:c.635G>A
|
ENSP00000500814.2:p.Arg212His
|
|
ENST00000674861.1:n.698G>A
|
|
|
ENST00000463290.5:c.635G>A
|
ENSP00000431538.1:p.Arg212His
|
|
ENST00000476410.1:n.95G>A
|
|
|
ENST00000488271.1:n.73G>A
|
|
|
ENST00000491222.5:c.47G>A
|
ENSP00000431441.1:p.Arg16His
|
|
ENST00000526189.2:c.298G>A
|
|
|
ENST00000533357.4:c.635G>A
|
ENSP00000432943.1:p.Arg212His
|
|
NM_000530.6:c.635G>A , LRG_256t1:c.635G>A
|
NP_000521.2:p.Arg212His
|
|
NM_000530.7:c.635G>A
|
NP_000521.2:p.Arg212His
|
|
NM_001315491.1:c.635G>A
|
NP_001302420.1:p.Arg212His
|
|
XM_017001321.2:c.665G>A
|
XP_016856810.1:p.Arg222His
|
|
NM_000530.8:c.635G>A
MANE Select
|
NP_000521.2:p.Arg212His
|
|
NM_001315491.2:c.635G>A
|
NP_001302420.1:p.Arg212His
|
|