ENST00000258385.8:c.1190G=
MANE Select
|
ENSP00000258385.3:p.Ser397=
|
|
ENST00000258385.7:c.1190G=
|
ENSP00000258385.3:p.Ser397=
|
|
ENST00000441621.6:c.*372G=
|
ENSP00000408819.2:n.*372G=
|
|
ENST00000446616.1:c.*831G=
|
ENSP00000410801.1:n.*831G=
|
|
ENST00000543200.5:c.1145G=
|
ENSP00000438380.1:p.Ser382=
|
|
NM_000751.2:c.1190G=
|
NP_000742.1:p.Ser397=
|
|
NM_001256657.1:c.1145G=
|
NP_001243586.1:p.Ser382=
|
|
NM_001311195.1:c.608G=
|
NP_001298124.1:p.Ser203=
|
|
NM_001311196.1:c.887G=
|
NP_001298125.1:p.Ser296=
|
|
NR_046333.1:c.-4294966361G=
|
|
|
NR_046334.1:c.-4294966082G=
|
|
|
XM_011510524.1:c.809G=
|
XP_011508826.1:p.Ser270=
|
|
XM_011510524.2:c.809G=
|
XP_011508826.1:p.Ser270=
|
|
NM_000751.3:c.1190G=
MANE Select
|
NP_000742.1:p.Ser397=
|
|
NM_001311195.2:c.608G=
|
NP_001298124.1:p.Ser203=
|
|
NM_001311196.2:c.887G=
|
NP_001298125.1:p.Ser296=
|
|
NM_001256657.2:c.1145G=
|
NP_001243586.1:p.Ser382=
|
|