ENST00000290866.10:c.402G=
MANE Select
|
ENSP00000290866.4:p.Leu134=
|
|
ENST00000290866.9:c.402G=
|
ENSP00000290866.4:p.Leu134=
|
|
ENST00000428043.5:c.402G=
|
ENSP00000397593.2:p.Leu134=
|
|
ENST00000579462.1:n.427G=
|
|
|
ENST00000580318.1:n.591G=
|
|
|
ENST00000582627.1:c.402G=
|
ENSP00000462280.1:p.Leu134=
|
|
ENST00000582678.5:c.402G=
|
ENSP00000462995.1:p.Leu134=
|
|
ENST00000583336.5:n.436G=
|
|
|
ENST00000584529.5:n.436G=
|
|
|
NM_000789.3:c.402G=
|
NP_000780.1:p.Leu134=
|
|
XM_005257110.1:c.-54G=
|
XP_005257167.1:n.-54G=
|
|
NM_000789.4:c.402G=
MANE Select
|
NP_000780.1:p.Leu134=
|
|
NM_001382700.1:c.167G=
|
NP_001369629.1:p.Trp56=
|
|
NM_001382701.1:c.-213G=
|
NP_001369630.1:n.-213G=
|
|