ENST00000326139.7:c.*221T>C
MANE Select
|
ENSP00000320180.2:n.*221T>C
|
|
ENST00000326139.6:c.*221T>C
|
ENSP00000320180.2:n.*221T>C
|
|
ENST00000337750.9:c.*709T>C
|
ENSP00000338184.4:n.*709T>C
|
|
ENST00000396227.6:c.*709T>C
|
ENSP00000379529.2:n.*709T>C
|
|
ENST00000409316.5:c.*336T>C
|
ENSP00000386602.1:n.*336T>C
|
|
ENST00000409904.7:c.*221T>C
|
ENSP00000387113.3:n.*221T>C
|
|
ENST00000461424.5:n.680+2907T>C
|
|
|
ENST00000463164.1:n.477T>C
|
|
|
ENST00000611037.1:c.550+2907T>C
|
ENSP00000480159.1:n.550+2907T>C
|
|
NM_000823.3:c.*221T>C
|
NP_000814.2:n.*221T>C
|
|
XM_011515263.1:c.*221T>C
|
XP_011513565.1:n.*221T>C
|
|
NM_000823.4:c.*221T>C
MANE Select
|
NP_000814.2:n.*221T>C
|
|