ENST00000699947.1:c.433G>C
|
ENSP00000514703.1:p.Asp145His
|
|
ENST00000699948.1:c.433G>C
|
ENSP00000514704.1:p.Asp145His
|
|
ENST00000699950.1:n.385G>C
|
|
|
ENST00000382745.9:c.433G>C
MANE Select
|
ENSP00000372193.4:p.Asp145His
|
|
ENST00000262318.12:c.361G>C
|
ENSP00000262318.8:p.Asp121His
|
|
ENST00000382745.8:c.433G>C
|
ENSP00000372193.4:p.Asp145His
|
|
ENST00000448525.5:c.361G>C
|
ENSP00000410907.1:p.Asp121His
|
|
ENST00000561665.5:n.463G>C
|
|
|
ENST00000564568.1:c.328G>C
|
ENSP00000454845.1:p.Asp110His
|
|
ENST00000567139.1:n.484G>C
|
|
|
ENST00000569851.6:c.259G>C
|
ENSP00000461009.1:p.Asp87His
|
|
NM_001114331.2:c.361G>C
|
NP_001107803.1:p.Asp121His
|
|
NM_001287.5:c.433G>C
|
NP_001278.1:p.Asp145His
|
|
XM_011522354.1:c.259G>C
|
XP_011520656.1:p.Asp87His
|
|
NM_001287.6:c.433G>C
MANE Select
|
NP_001278.1:p.Asp145His
|
|
NM_001114331.3:c.361G>C
|
NP_001107803.1:p.Asp121His
|
|