ENST00000647956.2:c.1039-133C>T
MANE Select
|
ENSP00000497341.1:n.1039-133C>T
|
|
ENST00000648162.1:n.1011-133C>T
|
|
|
ENST00000649804.1:c.133-133C>T
|
ENSP00000497938.1:n.133-133C>T
|
|
ENST00000535233.6:c.937-133C>T
|
ENSP00000438636.3:n.937-133C>T
|
|
ENST00000536053.6:c.1081-133C>T
|
ENSP00000444271.3:n.1081-133C>T
|
|
ENST00000540394.5:n.2104-133C>T
|
|
|
ENST00000542285.5:c.1039-133C>T
|
ENSP00000438615.2:n.1039-133C>T
|
|
ENST00000602298.2:n.1255C>T
|
|
|
NM_001733.4:c.1039-133C>T
|
NP_001724.3:n.1039-133C>T
|
|
NM_001354346.1:c.1081-133C>T
|
NP_001341275.1:n.1081-133C>T
|
|
NM_001733.6:c.1039-133C>T
|
NP_001724.4:n.1039-133C>T
|
|
NM_001733.7:c.1039-133C>T
MANE Select
|
NP_001724.4:n.1039-133C>T
|
|
NM_001354346.2:c.1081-133C>T
|
NP_001341275.1:n.1081-133C>T
|
|