ENST00000290866.10:c.3616G>C
MANE Select
|
ENSP00000290866.4:p.Asp1206His
|
|
ENST00000290863.10:c.1894G>C
|
ENSP00000290863.6:p.Asp632His
|
|
ENST00000290866.9:c.3616G>C
|
ENSP00000290866.4:p.Asp1206His
|
|
ENST00000413513.7:c.1771G>C
|
ENSP00000392247.3:p.Asp591His
|
|
ENST00000428043.5:c.3616G>C
|
ENSP00000397593.2:p.Asp1206His
|
|
ENST00000577418.5:n.626G>C
|
|
|
ENST00000577647.2:c.1894G>C
|
ENSP00000464149.1:p.Asp632His
|
|
ENST00000578839.5:c.*1371G>C
|
ENSP00000462110.2:n.*1371G>C
|
|
ENST00000579314.5:c.*1345G>C
|
ENSP00000462599.1:n.*1345G>C
|
|
ENST00000579409.1:c.303G>C
|
|
|
ENST00000582244.1:n.490G>C
|
|
|
NM_000789.3:c.3616G>C
|
NP_000780.1:p.Asp1206His
|
|
NM_001178057.1:c.1771G>C
|
NP_001171528.1:p.Asp591His
|
|
NM_152830.2:c.1894G>C
|
NP_690043.1:p.Asp632His
|
|
XM_005257110.1:c.3067G>C
|
XP_005257167.1:p.Asp1023His
|
|
XM_006721737.2:c.1954G>C
|
XP_006721800.2:p.Asp652His
|
|
XM_006721737.3:c.1954G>C
|
XP_006721800.2:p.Asp652His
|
|
NM_000789.4:c.3616G>C
MANE Select
|
NP_000780.1:p.Asp1206His
|
|
NM_001178057.2:c.1771G>C
|
NP_001171528.1:p.Asp591His
|
|
NM_152830.3:c.1894G>C
|
NP_690043.1:p.Asp632His
|
|
NM_001382700.1:c.3049G>C
|
NP_001369629.1:p.Asp1017His
|
|
NM_001382701.1:c.2764G>C
|
NP_001369630.1:p.Asp922His
|
|
NM_001382702.1:c.1231G>C
|
NP_001369631.1:p.Asp411His
|
|
NR_168483.1:n.1994G>C
|
|
|