ENST00000325455.10:c.*4262A>G
MANE Select
|
ENSP00000325120.5:n.*4262A>G
|
|
ENST00000325455.9:c.*4262A>G
|
ENSP00000325120.5:n.*4262A>G
|
|
NM_000926.4:c.*4262A>G
MANE Select
|
NP_000917.3:n.*4262A>G
|
|
NM_001202474.3:c.*4262A>G
|
NP_001189403.1:n.*4262A>G
|
|
NM_001271161.2:c.*4262A>G
|
NP_001258090.1:n.*4262A>G
|
|
NM_001271162.1:c.*4262A>G
|
NP_001258091.1:n.*4262A>G
|
|
NR_073141.2:n.7005A>G
|
|
|
NR_073142.2:n.6888A>G
|
|
|
NR_073143.2:n.6620A>G
|
|
|
NM_001271162.2:c.*4262A>G
|
NP_001258091.1:n.*4262A>G
|
|
NR_073141.3:n.7019A>G
|
|
|
NR_073142.3:n.6902A>G
|
|
|
NR_073143.3:n.6634A>G
|
|
|