ENST00000290866.10:c.1119-1G>T
MANE Select
|
ENSP00000290866.4:n.1119-1G>T
|
|
ENST00000290866.9:c.1119-1G>T
|
ENSP00000290866.4:n.1119-1G>T
|
|
ENST00000428043.5:c.1119-1G>T
|
ENSP00000397593.2:n.1119-1G>T
|
|
ENST00000582678.5:c.*518-1G>T
|
ENSP00000462995.1:n.*518-1G>T
|
|
ENST00000584529.5:n.1153-1G>T
|
|
|
NM_000789.3:c.1119-1G>T
|
NP_000780.1:n.1119-1G>T
|
|
XM_005257110.1:c.570-1G>T
|
XP_005257167.1:n.570-1G>T
|
|
NM_000789.4:c.1119-1G>T
MANE Select
|
NP_000780.1:n.1119-1G>T
|
|
NM_001382700.1:c.551G>T
|
NP_001369629.1:p.Arg184Met
|
|
NM_001382701.1:c.267-1G>T
|
NP_001369630.1:n.267-1G>T
|
|