|
ENST00000588981.6:c.200A>G
MANE Select
|
ENSP00000467176.1:p.His67Arg
|
|
|
ENST00000291901.12:c.200A>G
|
ENSP00000291901.8:p.His67Arg
|
|
|
ENST00000356783.9:c.167A>G
|
ENSP00000349233.4:p.His56Arg
|
|
|
ENST00000536926.5:c.-11A>G
|
ENSP00000439640.2:n.-11A>G
|
|
|
ENST00000585321.6:c.-11A>G
|
ENSP00000467980.2:n.-11A>G
|
|
|
ENST00000587089.6:c.252A>G
|
|
|
|
ENST00000587465.6:c.-11A>G
|
ENSP00000464843.2:n.-11A>G
|
|
|
ENST00000587758.5:c.167A>G
|
ENSP00000467789.1:p.His56Arg
|
|
|
ENST00000588147.5:c.188A>G
|
ENSP00000467299.1:p.His63Arg
|
|
|
ENST00000588426.5:c.49-383A>G
|
ENSP00000465991.1:n.49-383A>G
|
|
|
ENST00000588981.5:c.200A>G
|
ENSP00000467176.1:p.His67Arg
|
|
|
ENST00000589226.5:c.167A>G
|
ENSP00000470854.1:p.His56Arg
|
|
|
ENST00000592920.5:n.278A>G
|
|
|
|
ENST00000593046.5:c.200A>G
|
ENSP00000470777.1:p.His67Arg
|
|
|
ENST00000593194.5:c.43A>G
|
|
|
|
NM_001126132.2:c.200A>G
|
NP_001119604.1:p.His67Arg
|
|
|
NM_001126133.2:c.167A>G
|
NP_001119605.1:p.His56Arg
|
|
|
NM_001291774.1:c.167A>G
|
NP_001278703.1:p.His56Arg
|
|
|
NM_003283.5:c.200A>G
|
NP_003274.3:p.His67Arg
|
|
|
XM_006723343.2:c.236A>G
|
XP_006723406.1:p.His79Arg
|
|
|
XM_011527243.1:c.224A>G
|
XP_011525545.1:p.His75Arg
|
|
|
XM_011527244.1:c.203A>G
|
XP_011525546.1:p.His68Arg
|
|
|
XM_011527245.1:c.200A>G
|
XP_011525547.1:p.His67Arg
|
|
|
XM_011527246.1:c.188A>G
|
XP_011525548.1:p.His63Arg
|
|
|
XM_011527246.3:c.188A>G
|
XP_011525548.1:p.His63Arg
|
|
|
XM_017027186.1:c.200A>G
|
XP_016882675.1:p.His67Arg
|
|
|
XM_017027187.1:c.188A>G
|
XP_016882676.1:p.His63Arg
|
|
|
NM_003283.6:c.200A>G
MANE Select
|
NP_003274.3:p.His67Arg
|
|
|
NM_001126132.3:c.200A>G
|
NP_001119604.1:p.His67Arg
|
|
|
NM_001126133.3:c.167A>G
|
NP_001119605.1:p.His56Arg
|
|
|
NM_001291774.2:c.167A>G
|
NP_001278703.1:p.His56Arg
|
|
