ENST00000290866.10:c.249+211G>C
MANE Select
|
ENSP00000290866.4:n.249+211G>C
|
|
ENST00000290866.9:c.249+211G>C
|
ENSP00000290866.4:n.249+211G>C
|
|
ENST00000428043.5:c.249+211G>C
|
ENSP00000397593.2:n.249+211G>C
|
|
ENST00000579462.1:n.274+211G>C
|
|
|
ENST00000580318.1:n.62G>C
|
|
|
ENST00000582627.1:c.13G>C
|
ENSP00000462280.1:p.Gly5Arg
|
|
ENST00000582678.5:c.249+211G>C
|
ENSP00000462995.1:n.249+211G>C
|
|
ENST00000583336.5:n.283+211G>C
|
|
|
ENST00000584529.5:n.283+211G>C
|
|
|
NM_000789.3:c.249+211G>C
|
NP_000780.1:n.249+211G>C
|
|
XM_005257110.1:c.-207+211G>C
|
XP_005257167.1:n.-207+211G>C
|
|
NM_000789.4:c.249+211G>C
MANE Select
|
NP_000780.1:n.249+211G>C
|
|
NM_001382700.1:c.14+211G>C
|
NP_001369629.1:n.14+211G>C
|
|
NM_001382701.1:c.-366+211G>C
|
NP_001369630.1:n.-366+211G>C
|
|