ENST00000290866.10:c.309G>T
MANE Select
|
ENSP00000290866.4:p.Glu103Asp
|
|
ENST00000290866.9:c.309G>T
|
ENSP00000290866.4:p.Glu103Asp
|
|
ENST00000428043.5:c.309G>T
|
ENSP00000397593.2:p.Glu103Asp
|
|
ENST00000579462.1:n.334G>T
|
|
|
ENST00000580318.1:n.498G>T
|
|
|
ENST00000582627.1:c.309G>T
|
ENSP00000462280.1:p.Glu103Asp
|
|
ENST00000582678.5:c.309G>T
|
ENSP00000462995.1:p.Glu103Asp
|
|
ENST00000583336.5:n.343G>T
|
|
|
ENST00000584529.5:n.343G>T
|
|
|
NM_000789.3:c.309G>T
|
NP_000780.1:p.Glu103Asp
|
|
XM_005257110.1:c.-147G>T
|
XP_005257167.1:n.-147G>T
|
|
NM_000789.4:c.309G>T
MANE Select
|
NP_000780.1:p.Glu103Asp
|
|
NM_001382700.1:c.74G>T
|
NP_001369629.1:p.Ser25Ile
|
|
NM_001382701.1:c.-306G>T
|
NP_001369630.1:n.-306G>T
|
|