ENST00000682012.1:n.545T=
|
|
|
ENST00000684569.1:n.515T=
|
|
|
ENST00000561421.6:c.470T=
MANE Select
|
ENSP00000453347.2:p.Val157=
|
|
ENST00000646551.1:n.2097T=
|
|
|
ENST00000261755.9:c.470T=
|
ENSP00000261755.5:p.Val157=
|
|
ENST00000407106.5:c.470T=
|
ENSP00000385080.1:p.Val157=
|
|
ENST00000539156.5:c.260T=
|
ENSP00000454271.1:p.Val87=
|
|
ENST00000558022.5:c.470T=
|
ENSP00000453152.1:p.Val157=
|
|
ENST00000558514.1:n.16T=
|
|
|
ENST00000558627.1:n.398T=
|
|
|
ENST00000561421.5:c.470T=
|
ENSP00000453347.1:p.Val157=
|
|
NM_000137.2:c.470T=
|
NP_000128.1:p.Val157=
|
|
XM_024449872.1:c.470T=
|
XP_024305640.1:p.Val157=
|
|
NM_000137.4:c.470T=
MANE Select
|
NP_000128.1:p.Val157=
|
|
NM_001374377.1:c.470T=
|
NP_001361306.1:p.Val157=
|
|
NM_001374380.1:c.470T=
|
NP_001361309.1:p.Val157=
|
|