ENST00000478723.6:n.244T>G
|
|
|
ENST00000482363.2:n.1340T>G
|
|
|
ENST00000485675.2:n.1334T>G
|
|
|
ENST00000688055.1:c.173T>G
|
ENSP00000508688.1:p.Met58Arg
|
|
ENST00000382564.8:c.173T>G
MANE Select
|
ENSP00000372005.2:p.Met58Arg
|
|
ENST00000643241.1:c.98T>G
|
ENSP00000496401.1:p.Met33Arg
|
|
ENST00000646965.1:c.-46-983T>G
|
ENSP00000496456.1:n.-46-983T>G
|
|
ENST00000382564.6:c.173T>G
|
ENSP00000372005.2:p.Met58Arg
|
|
ENST00000469657.5:c.130-983T>G
|
ENSP00000418058.1:n.130-983T>G
|
|
ENST00000478723.5:n.312T>G
|
|
|
ENST00000479269.5:c.98T>G
|
ENSP00000419191.1:p.Met33Arg
|
|
ENST00000485675.1:n.1246T>G
|
|
|
ENST00000486355.1:c.154+19T>G
|
ENSP00000419991.1:n.154+19T>G
|
|
ENST00000491873.5:c.98T>G
|
ENSP00000420767.1:p.Met33Arg
|
|
NM_001190233.1:c.98T>G
|
NP_001177162.1:p.Met33Arg
|
|
NM_145261.3:c.173T>G
|
NP_660304.1:p.Met58Arg
|
|
NR_033721.1:n.293T>G
|
|
|
NR_033722.1:n.302-983T>G
|
|
|
NR_033723.1:n.326+19T>G
|
|
|
NR_046073.1:n.176-983T>G
|
|
|
NM_145261.4:c.173T>G
MANE Select
|
NP_660304.1:p.Met58Arg
|
|
NM_001190233.2:c.98T>G
|
NP_001177162.1:p.Met33Arg
|
|
NR_033721.2:n.255T>G
|
|
|
NR_033722.2:n.264-983T>G
|
|
|