ENST00000698881.1:c.1170A>C
|
ENSP00000514003.1:p.Gln390His
|
|
ENST00000418331.7:c.828A>C
MANE Select
|
ENSP00000400010.2:p.Gln276His
|
|
ENST00000418331.6:c.828A>C
|
ENSP00000400010.2:p.Gln276His
|
|
ENST00000440289.6:c.828A>C
|
ENSP00000409733.2:p.Gln276His
|
|
ENST00000613246.4:c.828A>C
|
ENSP00000477933.1:p.Gln276His
|
|
ENST00000615445.4:c.828A>C
|
ENSP00000479342.1:p.Gln276His
|
|
NM_001098503.1:c.828A>C
|
NP_001091973.1:p.Gln276His
|
|
NM_002843.3:c.828A>C
|
NP_002834.3:p.Gln276His
|
|
XM_011520249.1:c.861A>C
|
XP_011518551.1:p.Gln287His
|
|
XR_930883.1:n.1178A>C
|
|
|
XM_017018083.1:c.906A>C
|
XP_016873572.1:p.Gln302His
|
|
XM_017018084.1:c.849A>C
|
XP_016873573.1:p.Gln283His
|
|
XM_017018085.1:c.780A>C
|
XP_016873574.1:p.Gln260His
|
|
XR_930883.2:n.1237A>C
|
|
|
NM_002843.4:c.828A>C
MANE Select
|
NP_002834.3:p.Gln276His
|
|
NM_001098503.2:c.828A>C
|
NP_001091973.1:p.Gln276His
|
|