ENST00000290866.10:c.3861C>G
MANE Select
|
ENSP00000290866.4:p.Ser1287Arg
|
|
ENST00000290863.10:c.2139C>G
|
ENSP00000290863.6:p.Ser713Arg
|
|
ENST00000290866.9:c.3861C>G
|
ENSP00000290866.4:p.Ser1287Arg
|
|
ENST00000413513.7:c.2016C>G
|
ENSP00000392247.3:p.Ser672Arg
|
|
ENST00000428043.5:c.*283C>G
|
ENSP00000397593.2:n.*283C>G
|
|
ENST00000577647.2:c.1969+321C>G
|
ENSP00000464149.1:n.1969+321C>G
|
|
ENST00000578839.5:c.*1616C>G
|
ENSP00000462110.2:n.*1616C>G
|
|
ENST00000579314.5:c.*1590C>G
|
ENSP00000462599.1:n.*1590C>G
|
|
NM_000789.3:c.3861C>G
|
NP_000780.1:p.Ser1287Arg
|
|
NM_001178057.1:c.2016C>G
|
NP_001171528.1:p.Ser672Arg
|
|
NM_152830.2:c.2139C>G
|
NP_690043.1:p.Ser713Arg
|
|
XM_005257110.1:c.3312C>G
|
XP_005257167.1:p.Ser1104Arg
|
|
XM_006721737.2:c.2199C>G
|
XP_006721800.2:p.Ser733Arg
|
|
XM_006721737.3:c.2199C>G
|
XP_006721800.2:p.Ser733Arg
|
|
NM_000789.4:c.3861C>G
MANE Select
|
NP_000780.1:p.Ser1287Arg
|
|
NM_001178057.2:c.2016C>G
|
NP_001171528.1:p.Ser672Arg
|
|
NM_152830.3:c.2139C>G
|
NP_690043.1:p.Ser713Arg
|
|
NM_001382700.1:c.3294C>G
|
NP_001369629.1:p.Ser1098Arg
|
|
NM_001382701.1:c.3009C>G
|
NP_001369630.1:p.Ser1003Arg
|
|
NM_001382702.1:c.1476C>G
|
NP_001369631.1:p.Ser492Arg
|
|
NR_168483.1:n.2239C>G
|
|
|