ENST00000325455.10:c.*4456G>T
MANE Select
|
ENSP00000325120.5:n.*4456G>T
|
|
ENST00000325455.9:c.*4456G>T
|
ENSP00000325120.5:n.*4456G>T
|
|
NM_000926.4:c.*4456G>T
MANE Select
|
NP_000917.3:n.*4456G>T
|
|
NM_001202474.3:c.*4456G>T
|
NP_001189403.1:n.*4456G>T
|
|
NM_001271161.2:c.*4456G>T
|
NP_001258090.1:n.*4456G>T
|
|
NM_001271162.1:c.*4456G>T
|
NP_001258091.1:n.*4456G>T
|
|
NR_073141.2:n.7199G>T
|
|
|
NR_073142.2:n.7082G>T
|
|
|
NR_073143.2:n.6814G>T
|
|
|
NM_001271162.2:c.*4456G>T
|
NP_001258091.1:n.*4456G>T
|
|
NR_073141.3:n.7213G>T
|
|
|
NR_073142.3:n.7096G>T
|
|
|
NR_073143.3:n.6828G>T
|
|
|