ENST00000697953.1:n.283G=
|
|
|
ENST00000698015.1:n.29G=
|
|
|
ENST00000698016.1:c.254G=
|
ENSP00000513502.1:p.Arg85=
|
|
ENST00000698021.1:c.58G=
|
|
|
ENST00000698022.1:c.212G=
|
ENSP00000513504.1:p.Arg71=
|
|
ENST00000698027.1:c.254G=
|
ENSP00000513505.1:p.Arg85=
|
|
ENST00000448276.7:c.395G=
MANE Select
|
ENSP00000392617.2:p.Arg132=
|
|
ENST00000225742.13:c.170G=
|
ENSP00000225742.9:p.Arg57=
|
|
ENST00000323347.14:c.251G=
|
ENSP00000318451.10:p.Arg84=
|
|
ENST00000448276.6:c.395G=
|
ENSP00000392617.2:p.Arg132=
|
|
ENST00000577686.1:n.53-210G=
|
|
|
ENST00000580054.1:c.179G=
|
ENSP00000463793.1:p.Arg60=
|
|
ENST00000584400.5:c.217-210G=
|
ENSP00000464503.1:n.217-210G=
|
|
ENST00000613943.4:c.284G=
|
ENSP00000483605.1:p.Arg95=
|
|
NM_001098426.1:c.395G=
|
NP_001091896.1:p.Arg132=
|
|
XM_005257604.2:c.170G=
|
XP_005257661.2:p.Arg57=
|
|
NM_001330439.1:c.170G=
|
NP_001317368.1:p.Arg57=
|
|
NM_001330440.1:c.251G=
|
NP_001317369.1:p.Arg84=
|
|
NM_001098426.2:c.395G=
MANE Select
|
NP_001091896.1:p.Arg132=
|
|
NM_001330440.2:c.251G=
|
NP_001317369.1:p.Arg84=
|
|