ENST00000636168.2:c.25G>C
|
ENSP00000490338.2:p.Asp9His
|
|
ENST00000672640.1:c.25G>C
|
ENSP00000500507.1:p.Asp9His
|
|
ENST00000261007.9:c.589G>C
|
ENSP00000261007.5:p.Asp197His
|
|
ENST00000348749.9:c.514G>C
MANE Select
|
ENSP00000261008.5:p.Asp172His
|
|
ENST00000409219.5:c.514G>C
|
ENSP00000386611.1:p.Asp172His
|
|
ENST00000409323.1:c.514G>C
|
ENSP00000386684.1:p.Asp172His
|
|
ENST00000409542.5:c.268G>C
|
ENSP00000387026.1:p.Asp90His
|
|
ENST00000435083.5:c.*158G>C
|
ENSP00000395805.1:n.*158G>C
|
|
NM_000079.3:c.514G>C
|
NP_000070.1:p.Asp172His
|
|
NM_001039523.2:c.589G>C
|
NP_001034612.1:p.Asp197His
|
|
XM_017003256.1:c.610G>C
|
XP_016858745.1:p.Asp204His
|
|
XM_017003257.1:c.535G>C
|
XP_016858746.1:p.Asp179His
|
|
NM_000079.4:c.514G>C
MANE Select
|
NP_000070.1:p.Asp172His
|
|
NM_001039523.3:c.589G>C
|
NP_001034612.1:p.Asp197His
|
|