|
ENST00000455702.7:c.823G>C
|
ENSP00000402238.3:p.Asp275His
|
|
|
ENST00000367318.10:c.808G>C
|
ENSP00000356287.5:p.Asp270His
|
|
|
ENST00000367322.6:c.796G>C
|
ENSP00000356291.2:p.Asp266His
|
|
|
ENST00000412633.3:c.799G>C
|
ENSP00000408731.2:p.Asp267His
|
|
|
ENST00000422165.6:c.829G>C
|
ENSP00000395163.2:p.Asp277His
|
|
|
ENST00000438742.6:c.787G>C
|
ENSP00000414036.2:p.Asp263His
|
|
|
ENST00000651504.1:n.1299G>C
|
|
|
|
ENST00000656932.1:c.838G>C
MANE Select
|
ENSP00000499593.1:p.Asp280His
|
|
|
ENST00000658476.1:c.873G>C
|
ENSP00000499741.1:p.Thr291=
|
|
|
ENST00000660295.1:c.808G>C
|
ENSP00000499418.1:p.Asp270His
|
|
|
ENST00000662159.1:c.*197G>C
|
ENSP00000499796.1:n.*197G>C
|
|
|
ENST00000663843.1:c.*738G>C
|
ENSP00000499590.1:n.*738G>C
|
|
|
ENST00000666449.1:c.*83G>C
|
ENSP00000499667.1:n.*83G>C
|
|
|
ENST00000236918.11:c.838G>C
|
ENSP00000236918.8:p.Asp280His
|
|
|
ENST00000360372.8:c.709G>C
|
ENSP00000353535.5:p.Asp237His
|
|
|
ENST00000367315.6:c.817G>C
|
ENSP00000356284.3:p.Asp273His
|
|
|
ENST00000367317.8:c.790G>C
|
ENSP00000356286.5:p.Asp264His
|
|
|
ENST00000367318.9:c.808G>C
|
ENSP00000356287.5:p.Asp270His
|
|
|
ENST00000367320.6:c.709G>C
|
ENSP00000356289.2:p.Asp237His
|
|
|
ENST00000367322.5:c.799G>C
|
ENSP00000356291.1:p.Asp267His
|
|
|
ENST00000421663.6:c.622G>C
|
ENSP00000404134.3:p.Asp208His
|
|
|
ENST00000438742.5:c.790G>C
|
ENSP00000414036.1:p.Asp264His
|
|
|
ENST00000458432.6:c.622G>C
|
ENSP00000387874.3:p.Asp208His
|
|
|
ENST00000460780.5:n.1957G>C
|
|
|
|
ENST00000476888.5:n.255G>C
|
|
|
|
ENST00000491504.5:n.2047G>C
|
|
|
|
ENST00000509001.5:c.808G>C
|
ENSP00000422031.1:p.Asp270His
|
|
|
NM_000364.3:c.829G>C
|
NP_000355.2:p.Asp277His
|
|
|
NM_001001430.2:c.808G>C
|
NP_001001430.1:p.Asp270His
|
|
|
NM_001001431.2:c.799G>C
|
NP_001001431.1:p.Asp267His
|
|
|
NM_001001432.2:c.790G>C
|
NP_001001432.1:p.Asp264His
|
|
|
NM_001276345.1:c.838G>C
|
NP_001263274.1:p.Asp280His
|
|
|
NM_001276346.1:c.709G>C
|
NP_001263275.1:p.Asp237His
|
|
|
NM_001276347.1:c.808G>C
|
NP_001263276.1:p.Asp270His
|
|
|
XM_006711508.2:c.808G>C
|
XP_006711571.1:p.Asp270His
|
|
|
XM_006711509.2:c.805G>C
|
XP_006711572.1:p.Asp269His
|
|
|
XM_011509938.1:c.838G>C
|
XP_011508240.1:p.Asp280His
|
|
|
XM_011509939.1:c.835G>C
|
XP_011508241.1:p.Asp279His
|
|
|
XM_011509940.1:c.835G>C
|
XP_011508242.1:p.Asp279His
|
|
|
XM_011509941.1:c.832G>C
|
XP_011508243.1:p.Asp278His
|
|
|
XM_011509942.1:c.793G>C
|
XP_011508244.1:p.Asp265His
|
|
|
XM_011509943.1:c.793G>C
|
XP_011508245.1:p.Asp265His
|
|
|
XM_011509944.1:c.790G>C
|
XP_011508246.1:p.Asp264His
|
|
|
XM_011509946.1:c.631G>C
|
XP_011508248.1:p.Asp211His
|
|
|
XM_006711508.3:c.808G>C
|
XP_006711571.1:p.Asp270His
|
|
|
XM_006711509.3:c.805G>C
|
XP_006711572.1:p.Asp269His
|
|
|
XM_011509938.2:c.838G>C
|
XP_011508240.1:p.Asp280His
|
|
|
XM_011509940.2:c.835G>C
|
XP_011508242.1:p.Asp279His
|
|
|
XM_011509941.2:c.832G>C
|
XP_011508243.1:p.Asp278His
|
|
|
XM_011509942.2:c.793G>C
|
XP_011508244.1:p.Asp265His
|
|
|
XM_011509943.2:c.793G>C
|
XP_011508245.1:p.Asp265His
|
|
|
XM_011509944.2:c.790G>C
|
XP_011508246.1:p.Asp264His
|
|
|
XM_017002216.2:c.805G>C
|
XP_016857705.1:p.Asp269His
|
|
|
XM_017002217.1:c.799G>C
|
XP_016857706.1:p.Asp267His
|
|
|
XM_024449450.1:c.838G>C
|
XP_024305218.1:p.Asp280His
|
|
|
XM_024449454.1:c.805G>C
|
XP_024305222.1:p.Asp269His
|
|
|
XM_024449455.1:c.805G>C
|
XP_024305223.1:p.Asp269His
|
|
|
NM_000364.4:c.829G>C
|
NP_000355.2:p.Asp277His
|
|
|
NM_001001430.3:c.808G>C
|
NP_001001430.1:p.Asp270His
|
|
|
NM_001001431.3:c.799G>C
|
NP_001001431.1:p.Asp267His
|
|
|
NM_001001432.3:c.790G>C
|
NP_001001432.1:p.Asp264His
|
|
|
NM_001276345.2:c.838G>C
MANE Select
|
NP_001263274.1:p.Asp280His
|
|
|
NM_001276346.2:c.709G>C
|
NP_001263275.1:p.Asp237His
|
|
|
NM_001276347.2:c.808G>C
|
NP_001263276.1:p.Asp270His
|
|
