ENST00000290866.10:c.3847A=
MANE Select
|
ENSP00000290866.4:p.Ile1283=
|
|
ENST00000290863.10:c.2125A=
|
ENSP00000290863.6:p.Ile709=
|
|
ENST00000290866.9:c.3847A=
|
ENSP00000290866.4:p.Ile1283=
|
|
ENST00000413513.7:c.2002A=
|
ENSP00000392247.3:p.Ile668=
|
|
ENST00000428043.5:c.*269A=
|
ENSP00000397593.2:n.*269A=
|
|
ENST00000577647.2:c.1969+307A=
|
ENSP00000464149.1:n.1969+307A=
|
|
ENST00000578839.5:c.*1602A=
|
ENSP00000462110.2:n.*1602A=
|
|
ENST00000579314.5:c.*1576A=
|
ENSP00000462599.1:n.*1576A=
|
|
NM_000789.3:c.3847A=
|
NP_000780.1:p.Ile1283=
|
|
NM_001178057.1:c.2002A=
|
NP_001171528.1:p.Ile668=
|
|
NM_152830.2:c.2125A=
|
NP_690043.1:p.Ile709=
|
|
XM_005257110.1:c.3298A=
|
XP_005257167.1:p.Ile1100=
|
|
XM_006721737.2:c.2185A=
|
XP_006721800.2:p.Ile729=
|
|
XM_006721737.3:c.2185A=
|
XP_006721800.2:p.Ile729=
|
|
NM_000789.4:c.3847A=
MANE Select
|
NP_000780.1:p.Ile1283=
|
|
NM_001178057.2:c.2002A=
|
NP_001171528.1:p.Ile668=
|
|
NM_152830.3:c.2125A=
|
NP_690043.1:p.Ile709=
|
|
NM_001382700.1:c.3280A=
|
NP_001369629.1:p.Ile1094=
|
|
NM_001382701.1:c.2995A=
|
NP_001369630.1:p.Ile999=
|
|
NM_001382702.1:c.1462A=
|
NP_001369631.1:p.Ile488=
|
|
NR_168483.1:n.2225A=
|
|
|