NM_018490.5:c.376C>T
MANE Select
|
NP_060960.2:p.Arg126Ter
|
ENST00000379214.9:c.376C>T
MANE Select
|
ENSP00000368516.4:p.Arg126Ter
|
NM_001346432.1:c.304C>T
|
NP_001333361.1:p.Arg102Ter
|
NM_001346432.2:c.304C>T
|
NP_001333361.1:p.Arg102Ter
|
NM_018490.2:c.376C>T
|
NP_060960.2:p.Arg126Ter
|
NM_018490.3:c.376C>T
|
NP_060960.2:p.Arg126Ter
|
NM_018490.4:c.376C>T
|
NP_060960.2:p.Arg126Ter
|
ENST00000379214.8:c.376C>T
|
ENSP00000368516.4:p.Arg126Ter
|
ENST00000389858.4:c.304C>T
|
ENSP00000374508.4:p.Arg102Ter
|
ENST00000480977.2:c.258-5651C>T
|
ENSP00000431650.1:n.258-5651C>T
|