ENST00000325455.10:c.*4296C>T
MANE Select
|
ENSP00000325120.5:n.*4296C>T
|
|
ENST00000325455.9:c.*4296C>T
|
ENSP00000325120.5:n.*4296C>T
|
|
NM_000926.4:c.*4296C>T
MANE Select
|
NP_000917.3:n.*4296C>T
|
|
NM_001202474.3:c.*4296C>T
|
NP_001189403.1:n.*4296C>T
|
|
NM_001271161.2:c.*4296C>T
|
NP_001258090.1:n.*4296C>T
|
|
NM_001271162.1:c.*4296C>T
|
NP_001258091.1:n.*4296C>T
|
|
NR_073141.2:n.7039C>T
|
|
|
NR_073142.2:n.6922C>T
|
|
|
NR_073143.2:n.6654C>T
|
|
|
NM_001271162.2:c.*4296C>T
|
NP_001258091.1:n.*4296C>T
|
|
NR_073141.3:n.7053C>T
|
|
|
NR_073142.3:n.6936C>T
|
|
|
NR_073143.3:n.6668C>T
|
|
|