ENST00000290866.10:c.3763G>T
MANE Select
|
ENSP00000290866.4:p.Ala1255Ser
|
|
ENST00000290863.10:c.2041G>T
|
ENSP00000290863.6:p.Ala681Ser
|
|
ENST00000290866.9:c.3763G>T
|
ENSP00000290866.4:p.Ala1255Ser
|
|
ENST00000413513.7:c.1918G>T
|
ENSP00000392247.3:p.Ala640Ser
|
|
ENST00000428043.5:c.*185G>T
|
ENSP00000397593.2:n.*185G>T
|
|
ENST00000577647.2:c.1969+223G>T
|
ENSP00000464149.1:n.1969+223G>T
|
|
ENST00000578839.5:c.*1518G>T
|
ENSP00000462110.2:n.*1518G>T
|
|
ENST00000579314.5:c.*1492G>T
|
ENSP00000462599.1:n.*1492G>T
|
|
NM_000789.3:c.3763G>T
|
NP_000780.1:p.Ala1255Ser
|
|
NM_001178057.1:c.1918G>T
|
NP_001171528.1:p.Ala640Ser
|
|
NM_152830.2:c.2041G>T
|
NP_690043.1:p.Ala681Ser
|
|
XM_005257110.1:c.3214G>T
|
XP_005257167.1:p.Ala1072Ser
|
|
XM_006721737.2:c.2101G>T
|
XP_006721800.2:p.Ala701Ser
|
|
XM_006721737.3:c.2101G>T
|
XP_006721800.2:p.Ala701Ser
|
|
NM_000789.4:c.3763G>T
MANE Select
|
NP_000780.1:p.Ala1255Ser
|
|
NM_001178057.2:c.1918G>T
|
NP_001171528.1:p.Ala640Ser
|
|
NM_152830.3:c.2041G>T
|
NP_690043.1:p.Ala681Ser
|
|
NM_001382700.1:c.3196G>T
|
NP_001369629.1:p.Ala1066Ser
|
|
NM_001382701.1:c.2911G>T
|
NP_001369630.1:p.Ala971Ser
|
|
NM_001382702.1:c.1378G>T
|
NP_001369631.1:p.Ala460Ser
|
|
NR_168483.1:n.2141G>T
|
|
|