ENST00000565588.6:c.343G=
|
ENSP00000455537.2:p.Ala115=
|
|
ENST00000696156.1:c.259G=
|
ENSP00000512446.1:p.Ala87=
|
|
ENST00000696157.1:c.343G=
|
ENSP00000512447.1:p.Ala115=
|
|
ENST00000696158.1:c.343G=
|
ENSP00000512448.1:p.Ala115=
|
|
ENST00000696159.1:c.343G=
|
ENSP00000512449.1:p.Ala115=
|
|
ENST00000696160.1:c.343G=
|
ENSP00000512450.1:p.Ala115=
|
|
ENST00000696161.1:c.473G=
|
ENSP00000512451.1:p.Gly158=
|
|
ENST00000696162.1:c.343G=
|
ENSP00000512452.1:p.Ala115=
|
|
ENST00000696163.1:c.292G=
|
ENSP00000512453.1:p.Ala98=
|
|
ENST00000261623.8:c.343G=
MANE Select
|
ENSP00000261623.3:p.Ala115=
|
|
ENST00000261623.7:c.343G=
|
ENSP00000261623.3:p.Ala115=
|
|
ENST00000562209.1:n.623G=
|
|
|
ENST00000563526.5:n.875G=
|
|
|
ENST00000565588.5:c.127G=
|
|
|
ENST00000566229.1:c.332G=
|
ENSP00000457060.1:p.Gly111=
|
|
ENST00000566534.5:n.922G=
|
|
|
ENST00000567174.5:c.343G=
|
ENSP00000454951.1:p.Ala115=
|
|
ENST00000568278.1:c.427G=
|
ENSP00000455506.1:p.Ala143=
|
|
ENST00000569359.5:c.343G=
|
ENSP00000456079.1:p.Ala115=
|
|
NM_000101.3:c.343G=
|
NP_000092.2:p.Ala115=
|
|
XM_011522905.1:c.343G=
|
XP_011521207.1:p.Ala115=
|
|
XM_011522905.3:c.343G=
|
XP_011521207.1:p.Ala115=
|
|
NM_000101.4:c.343G=
MANE Select
|
NP_000092.2:p.Ala115=
|
|