ENST00000340855.11:c.1615T=
MANE Select
|
ENSP00000339801.6:p.Ser539=
|
|
ENST00000651111.1:c.982T=
|
ENSP00000498395.1:p.Ser328=
|
|
ENST00000340855.10:c.1615T=
|
ENSP00000339801.6:p.Ser539=
|
|
ENST00000422081.6:c.982T=
|
ENSP00000477056.1:p.Ser328=
|
|
NM_000202.6:c.1615T=
|
NP_000193.1:p.Ser539=
|
|
NM_001166550.2:c.1345T=
|
NP_001160022.1:p.Ser449=
|
|
NM_000202.7:c.1615T=
|
NP_000193.1:p.Ser539=
|
|
NM_001166550.3:c.1345T=
|
NP_001160022.1:p.Ser449=
|
|
NM_000202.8:c.1615T=
MANE Select
|
NP_000193.1:p.Ser539=
|
|
NM_001166550.4:c.1345T=
|
NP_001160022.1:p.Ser449=
|
|