ENST00000290866.10:c.250-275T>G
MANE Select
|
ENSP00000290866.4:n.250-275T>G
|
|
ENST00000290866.9:c.250-275T>G
|
ENSP00000290866.4:n.250-275T>G
|
|
ENST00000428043.5:c.250-275T>G
|
ENSP00000397593.2:n.250-275T>G
|
|
ENST00000579462.1:n.275-275T>G
|
|
|
ENST00000580318.1:n.164T>G
|
|
|
ENST00000582627.1:c.115T>G
|
ENSP00000462280.1:p.Cys39Gly
|
|
ENST00000582678.5:c.250-275T>G
|
ENSP00000462995.1:n.250-275T>G
|
|
ENST00000583336.5:n.284-275T>G
|
|
|
ENST00000584529.5:n.284-275T>G
|
|
|
NM_000789.3:c.250-275T>G
|
NP_000780.1:n.250-275T>G
|
|
XM_005257110.1:c.-206-275T>G
|
XP_005257167.1:n.-206-275T>G
|
|
NM_000789.4:c.250-275T>G
MANE Select
|
NP_000780.1:n.250-275T>G
|
|
NM_001382700.1:c.15-275T>G
|
NP_001369629.1:n.15-275T>G
|
|
NM_001382701.1:c.-365-275T>G
|
NP_001369630.1:n.-365-275T>G
|
|