ENST00000258385.8:c.1186C>G
MANE Select
|
ENSP00000258385.3:p.Arg396Gly
|
|
ENST00000258385.7:c.1186C>G
|
ENSP00000258385.3:p.Arg396Gly
|
|
ENST00000441621.6:c.*368C>G
|
ENSP00000408819.2:n.*368C>G
|
|
ENST00000446616.1:c.*827C>G
|
ENSP00000410801.1:n.*827C>G
|
|
ENST00000543200.5:c.1141C>G
|
ENSP00000438380.1:p.Arg381Gly
|
|
NM_000751.2:c.1186C>G
|
NP_000742.1:p.Arg396Gly
|
|
NM_001256657.1:c.1141C>G
|
NP_001243586.1:p.Arg381Gly
|
|
NM_001311195.1:c.604C>G
|
NP_001298124.1:p.Arg202Gly
|
|
NM_001311196.1:c.883C>G
|
NP_001298125.1:p.Arg295Gly
|
|
NR_046333.1:c.-4294966365C>G
|
|
|
NR_046334.1:c.-4294966086C>G
|
|
|
XM_011510524.1:c.805C>G
|
XP_011508826.1:p.Arg269Gly
|
|
XM_011510524.2:c.805C>G
|
XP_011508826.1:p.Arg269Gly
|
|
NM_000751.3:c.1186C>G
MANE Select
|
NP_000742.1:p.Arg396Gly
|
|
NM_001311195.2:c.604C>G
|
NP_001298124.1:p.Arg202Gly
|
|
NM_001311196.2:c.883C>G
|
NP_001298125.1:p.Arg295Gly
|
|
NM_001256657.2:c.1141C>G
|
NP_001243586.1:p.Arg381Gly
|
|