ENST00000361462.7:c.*303G>A
MANE Select
|
ENSP00000354917.2:n.*303G>A
|
|
ENST00000361462.6:c.*303G>A
|
ENSP00000354917.2:n.*303G>A
|
|
ENST00000361577.7:c.*303G>A
|
ENSP00000355045.3:n.*303G>A
|
|
ENST00000557423.5:c.*2468G>A
|
ENSP00000451829.1:n.*2468G>A
|
|
NM_001308120.1:c.*303G>A
|
NP_001295049.1:n.*303G>A
|
|
NM_015091.2:c.*303G>A
|
NP_055906.2:n.*303G>A
|
|
NM_015091.3:c.*303G>A
|
NP_055906.2:n.*303G>A
|
|
NR_131765.1:n.5688G>A
|
|
|
XM_011536571.1:c.*608G>A
|
XP_011534873.1:n.*608G>A
|
|
XM_017021098.1:c.*303G>A
|
XP_016876587.1:n.*303G>A
|
|
XM_017021099.1:c.*303G>A
|
XP_016876588.1:n.*303G>A
|
|
XR_001750194.1:n.5952G>A
|
|
|
XR_001750195.1:n.5595G>A
|
|
|
NM_001308120.2:c.*303G>A
MANE Select
|
NP_001295049.1:n.*303G>A
|
|
NM_015091.4:c.*303G>A
|
NP_055906.2:n.*303G>A
|
|
NR_131765.2:n.5688G>A
|
|
|