ENST00000326139.7:c.*209G>T
MANE Select
|
ENSP00000320180.2:n.*209G>T
|
|
ENST00000326139.6:c.*209G>T
|
ENSP00000320180.2:n.*209G>T
|
|
ENST00000337750.9:c.*697G>T
|
ENSP00000338184.4:n.*697G>T
|
|
ENST00000396227.6:c.*697G>T
|
ENSP00000379529.2:n.*697G>T
|
|
ENST00000409316.5:c.*324G>T
|
ENSP00000386602.1:n.*324G>T
|
|
ENST00000409904.7:c.*209G>T
|
ENSP00000387113.3:n.*209G>T
|
|
ENST00000461424.5:n.680+2895G>T
|
|
|
ENST00000463164.1:n.465G>T
|
|
|
ENST00000611037.1:c.550+2895G>T
|
ENSP00000480159.1:n.550+2895G>T
|
|
NM_000823.3:c.*209G>T
|
NP_000814.2:n.*209G>T
|
|
XM_011515263.1:c.*209G>T
|
XP_011513565.1:n.*209G>T
|
|
NM_000823.4:c.*209G>T
MANE Select
|
NP_000814.2:n.*209G>T
|
|