ENST00000290866.10:c.2196G>T
MANE Select
|
ENSP00000290866.4:p.Leu732=
|
|
ENST00000290863.10:c.474G>T
|
ENSP00000290863.6:p.Leu158=
|
|
ENST00000290866.9:c.2196G>T
|
ENSP00000290866.4:p.Leu732=
|
|
ENST00000413513.7:c.474G>T
|
ENSP00000392247.3:p.Leu158=
|
|
ENST00000428043.5:c.2196G>T
|
ENSP00000397593.2:p.Leu732=
|
|
ENST00000577647.2:c.474G>T
|
ENSP00000464149.1:p.Leu158=
|
|
ENST00000578839.5:c.*266G>T
|
ENSP00000462110.2:n.*266G>T
|
|
ENST00000579204.1:c.377G>T
|
ENSP00000464629.1:n.377G>T
|
|
ENST00000579314.5:c.474G>T
|
ENSP00000462599.1:p.Leu158=
|
|
ENST00000579726.5:c.758G>T
|
|
|
ENST00000582005.5:c.*116G>T
|
ENSP00000462002.1:n.*116G>T
|
|
NM_000789.3:c.2196G>T
|
NP_000780.1:p.Leu732=
|
|
NM_001178057.1:c.474G>T
|
NP_001171528.1:p.Leu158=
|
|
NM_152830.2:c.474G>T
|
NP_690043.1:p.Leu158=
|
|
XM_005257110.1:c.1647G>T
|
XP_005257167.1:p.Leu549=
|
|
XM_006721737.2:c.534G>T
|
XP_006721800.2:p.Leu178=
|
|
XM_006721737.3:c.534G>T
|
XP_006721800.2:p.Leu178=
|
|
NM_000789.4:c.2196G>T
MANE Select
|
NP_000780.1:p.Leu732=
|
|
NM_001178057.2:c.474G>T
|
NP_001171528.1:p.Leu158=
|
|
NM_152830.3:c.474G>T
|
NP_690043.1:p.Leu158=
|
|
NM_001382700.1:c.1629G>T
|
NP_001369629.1:p.Leu543=
|
|
NM_001382701.1:c.1344G>T
|
NP_001369630.1:p.Leu448=
|
|
NM_001382702.1:c.126G>T
|
NP_001369631.1:p.Leu42=
|
|
NR_168483.1:n.496G>T
|
|
|