ENST00000290866.10:c.3762G>C
MANE Select
|
ENSP00000290866.4:p.Gln1254His
|
|
ENST00000290863.10:c.2040G>C
|
ENSP00000290863.6:p.Gln680His
|
|
ENST00000290866.9:c.3762G>C
|
ENSP00000290866.4:p.Gln1254His
|
|
ENST00000413513.7:c.1917G>C
|
ENSP00000392247.3:p.Gln639His
|
|
ENST00000428043.5:c.*184G>C
|
ENSP00000397593.2:n.*184G>C
|
|
ENST00000577647.2:c.1969+222G>C
|
ENSP00000464149.1:n.1969+222G>C
|
|
ENST00000578839.5:c.*1517G>C
|
ENSP00000462110.2:n.*1517G>C
|
|
ENST00000579314.5:c.*1491G>C
|
ENSP00000462599.1:n.*1491G>C
|
|
NM_000789.3:c.3762G>C
|
NP_000780.1:p.Gln1254His
|
|
NM_001178057.1:c.1917G>C
|
NP_001171528.1:p.Gln639His
|
|
NM_152830.2:c.2040G>C
|
NP_690043.1:p.Gln680His
|
|
XM_005257110.1:c.3213G>C
|
XP_005257167.1:p.Gln1071His
|
|
XM_006721737.2:c.2100G>C
|
XP_006721800.2:p.Gln700His
|
|
XM_006721737.3:c.2100G>C
|
XP_006721800.2:p.Gln700His
|
|
NM_000789.4:c.3762G>C
MANE Select
|
NP_000780.1:p.Gln1254His
|
|
NM_001178057.2:c.1917G>C
|
NP_001171528.1:p.Gln639His
|
|
NM_152830.3:c.2040G>C
|
NP_690043.1:p.Gln680His
|
|
NM_001382700.1:c.3195G>C
|
NP_001369629.1:p.Gln1065His
|
|
NM_001382701.1:c.2910G>C
|
NP_001369630.1:p.Gln970His
|
|
NM_001382702.1:c.1377G>C
|
NP_001369631.1:p.Gln459His
|
|
NR_168483.1:n.2140G>C
|
|
|