ENST00000573725.2:c.*96G>T
|
ENSP00000460849.2:n.*96G>T
|
|
ENST00000703537.1:c.2852G>T
|
|
|
ENST00000703538.1:c.*6827G>T
|
ENSP00000515361.1:n.*6827G>T
|
|
ENST00000703539.1:n.3418G>T
|
|
|
ENST00000703540.1:c.*96G>T
|
ENSP00000515362.1:n.*96G>T
|
|
ENST00000304992.11:c.*96G>T
MANE Select
|
ENSP00000304350.6:n.*96G>T
|
|
ENST00000304992.10:c.*96G>T
|
ENSP00000304350.6:n.*96G>T
|
|
ENST00000571958.1:c.303G>T
|
|
|
ENST00000572621.5:c.*96G>T
|
ENSP00000460348.1:n.*96G>T
|
|
NM_006445.3:c.*96G>T
|
NP_006436.3:n.*96G>T
|
|
XM_024450537.1:c.*96G>T
|
XP_024306305.1:n.*96G>T
|
|
NM_006445.4:c.*96G>T
MANE Select
|
NP_006436.3:n.*96G>T
|
|