ENST00000478723.6:n.230G=
|
|
|
ENST00000482363.2:n.1326G=
|
|
|
ENST00000485675.2:n.1320G=
|
|
|
ENST00000688055.1:c.159G=
|
ENSP00000508688.1:p.Gly53=
|
|
ENST00000382564.8:c.159G=
MANE Select
|
ENSP00000372005.2:p.Gly53=
|
|
ENST00000643241.1:c.84G=
|
ENSP00000496401.1:p.Gly28=
|
|
ENST00000646965.1:c.-46-997G=
|
ENSP00000496456.1:n.-46-997G=
|
|
ENST00000382564.6:c.159G=
|
ENSP00000372005.2:p.Gly53=
|
|
ENST00000469657.5:c.130-997G=
|
ENSP00000418058.1:n.130-997G=
|
|
ENST00000478723.5:n.298G=
|
|
|
ENST00000479269.5:c.84G=
|
ENSP00000419191.1:p.Gly28=
|
|
ENST00000485675.1:n.1232G=
|
|
|
ENST00000486355.1:c.154+5G=
|
ENSP00000419991.1:n.154+5G=
|
|
ENST00000491873.5:c.84G=
|
ENSP00000420767.1:p.Gly28=
|
|
NM_001190233.1:c.84G=
|
NP_001177162.1:p.Gly28=
|
|
NM_145261.3:c.159G=
|
NP_660304.1:p.Gly53=
|
|
NR_033721.1:n.279G=
|
|
|
NR_033722.1:n.302-997G=
|
|
|
NR_033723.1:n.326+5G=
|
|
|
NR_046073.1:n.176-997G=
|
|
|
NM_145261.4:c.159G=
MANE Select
|
NP_660304.1:p.Gly53=
|
|
NM_001190233.2:c.84G=
|
NP_001177162.1:p.Gly28=
|
|
NR_033721.2:n.241G=
|
|
|
NR_033722.2:n.264-997G=
|
|
|