ENST00000290866.10:c.396G>C
MANE Select
|
ENSP00000290866.4:p.Leu132=
|
|
ENST00000290866.9:c.396G>C
|
ENSP00000290866.4:p.Leu132=
|
|
ENST00000428043.5:c.396G>C
|
ENSP00000397593.2:p.Leu132=
|
|
ENST00000579462.1:n.421G>C
|
|
|
ENST00000580318.1:n.585G>C
|
|
|
ENST00000582627.1:c.396G>C
|
ENSP00000462280.1:p.Leu132=
|
|
ENST00000582678.5:c.396G>C
|
ENSP00000462995.1:p.Leu132=
|
|
ENST00000583336.5:n.430G>C
|
|
|
ENST00000584529.5:n.430G>C
|
|
|
NM_000789.3:c.396G>C
|
NP_000780.1:p.Leu132=
|
|
XM_005257110.1:c.-60G>C
|
XP_005257167.1:n.-60G>C
|
|
NM_000789.4:c.396G>C
MANE Select
|
NP_000780.1:p.Leu132=
|
|
NM_001382700.1:c.161G>C
|
NP_001369629.1:p.Cys54Ser
|
|
NM_001382701.1:c.-219G>C
|
NP_001369630.1:n.-219G>C
|
|