ENST00000375784.8:c.*99G>T
MANE Select
|
ENSP00000364940.3:n.*99G>T
|
|
ENST00000375779.6:c.*99G>T
|
ENSP00000364934.2:n.*99G>T
|
|
ENST00000375780.6:c.*99G>T
|
ENSP00000364935.2:n.*99G>T
|
|
ENST00000375784.7:c.*99G>T
|
ENSP00000364940.3:n.*99G>T
|
|
ENST00000395892.5:c.*99G>T
|
ENSP00000379229.1:n.*99G>T
|
|
ENST00000616760.1:c.*99G>T
|
ENSP00000479808.1:n.*99G>T
|
|
NM_001287593.1:c.*99G>T
|
NP_001274522.1:n.*99G>T
|
|
NM_001287594.1:c.*99G>T
|
NP_001274523.1:n.*99G>T
|
|
NM_001288.4:c.*99G>T
|
NP_001279.2:n.*99G>T
|
|
NM_001287594.3:c.*99G>T
|
NP_001274523.1:n.*99G>T
|
|
NM_001288.5:c.*99G>T
|
NP_001279.2:n.*99G>T
|
|
NM_001288.6:c.*99G>T
MANE Select
|
NP_001279.2:n.*99G>T
|
|