ENST00000290866.10:c.3870G>C
MANE Select
|
ENSP00000290866.4:p.Arg1290=
|
|
ENST00000290863.10:c.2148G>C
|
ENSP00000290863.6:p.Arg716=
|
|
ENST00000290866.9:c.3870G>C
|
ENSP00000290866.4:p.Arg1290=
|
|
ENST00000413513.7:c.2025G>C
|
ENSP00000392247.3:p.Arg675=
|
|
ENST00000428043.5:c.*292G>C
|
ENSP00000397593.2:n.*292G>C
|
|
ENST00000577647.2:c.1969+330G>C
|
ENSP00000464149.1:n.1969+330G>C
|
|
ENST00000578839.5:c.*1625G>C
|
ENSP00000462110.2:n.*1625G>C
|
|
ENST00000579314.5:c.*1599G>C
|
ENSP00000462599.1:n.*1599G>C
|
|
NM_000789.3:c.3870G>C
|
NP_000780.1:p.Arg1290=
|
|
NM_001178057.1:c.2025G>C
|
NP_001171528.1:p.Arg675=
|
|
NM_152830.2:c.2148G>C
|
NP_690043.1:p.Arg716=
|
|
XM_005257110.1:c.3321G>C
|
XP_005257167.1:p.Arg1107=
|
|
XM_006721737.2:c.2208G>C
|
XP_006721800.2:p.Arg736=
|
|
XM_006721737.3:c.2208G>C
|
XP_006721800.2:p.Arg736=
|
|
NM_000789.4:c.3870G>C
MANE Select
|
NP_000780.1:p.Arg1290=
|
|
NM_001178057.2:c.2025G>C
|
NP_001171528.1:p.Arg675=
|
|
NM_152830.3:c.2148G>C
|
NP_690043.1:p.Arg716=
|
|
NM_001382700.1:c.3303G>C
|
NP_001369629.1:p.Arg1101=
|
|
NM_001382701.1:c.3018G>C
|
NP_001369630.1:p.Arg1006=
|
|
NM_001382702.1:c.1485G>C
|
NP_001369631.1:p.Arg495=
|
|
NR_168483.1:n.2248G>C
|
|
|