ENST00000422447.8:c.*184G>T
MANE Select
|
ENSP00000395337.3:n.*184G>T
|
|
ENST00000227157.8:c.*333G>T
|
ENSP00000227157.4:n.*333G>T
|
|
ENST00000375710.7:n.2050G>T
|
|
|
ENST00000379412.9:c.*184G>T
|
ENSP00000368722.5:n.*184G>T
|
|
ENST00000396222.6:c.*89G>T
|
ENSP00000379524.2:n.*89G>T
|
|
ENST00000422447.7:c.*184G>T
|
ENSP00000395337.3:n.*184G>T
|
|
ENST00000430553.6:c.*184G>T
|
ENSP00000406172.2:n.*184G>T
|
|
ENST00000538451.1:n.1070G>T
|
|
|
ENST00000540430.5:c.*184G>T
|
ENSP00000445175.1:n.*184G>T
|
|
ENST00000545215.5:c.*927G>T
|
ENSP00000442637.1:n.*927G>T
|
|
NM_001135239.1:c.*184G>T
|
NP_001128711.1:n.*184G>T
|
|
NM_001165414.1:c.*184G>T
|
NP_001158886.1:n.*184G>T
|
|
NM_001165415.1:c.*89G>T
|
NP_001158887.1:n.*89G>T
|
|
NM_001165416.1:c.*333G>T
|
NP_001158888.1:n.*333G>T
|
|
NM_005566.3:c.*184G>T
|
NP_005557.1:n.*184G>T
|
|
NR_028500.1:n.1337G>T
|
|
|
NM_005566.4:c.*184G>T
MANE Select
|
NP_005557.1:n.*184G>T
|
|
NM_001165415.2:c.*89G>T
|
NP_001158887.1:n.*89G>T
|
|
NM_001135239.2:c.*184G>T
|
NP_001128711.1:n.*184G>T
|
|
NM_001165414.2:c.*184G>T
|
NP_001158886.1:n.*184G>T
|
|
NM_001165416.2:c.*333G>T
|
NP_001158888.1:n.*333G>T
|
|
NR_028500.2:n.1163G>T
|
|
|