ENST00000258385.8:c.1333A>G
MANE Select
|
ENSP00000258385.3:p.Ile445Val
|
|
ENST00000258385.7:c.1333A>G
|
ENSP00000258385.3:p.Ile445Val
|
|
ENST00000441621.6:c.*515A>G
|
ENSP00000408819.2:n.*515A>G
|
|
ENST00000446616.1:c.*974A>G
|
ENSP00000410801.1:n.*974A>G
|
|
ENST00000543200.5:c.1288A>G
|
ENSP00000438380.1:p.Ile430Val
|
|
NM_000751.2:c.1333A>G
|
NP_000742.1:p.Ile445Val
|
|
NM_001256657.1:c.1288A>G
|
NP_001243586.1:p.Ile430Val
|
|
NM_001311195.1:c.751A>G
|
NP_001298124.1:p.Ile251Val
|
|
NM_001311196.1:c.1030A>G
|
NP_001298125.1:p.Ile344Val
|
|
NR_046333.1:c.-4294966218A>G
|
|
|
NR_046334.1:c.-4294965939A>G
|
|
|
XM_011510524.1:c.952A>G
|
XP_011508826.1:p.Ile318Val
|
|
XM_011510524.2:c.952A>G
|
XP_011508826.1:p.Ile318Val
|
|
NM_000751.3:c.1333A>G
MANE Select
|
NP_000742.1:p.Ile445Val
|
|
NM_001311195.2:c.751A>G
|
NP_001298124.1:p.Ile251Val
|
|
NM_001311196.2:c.1030A>G
|
NP_001298125.1:p.Ile344Val
|
|
NM_001256657.2:c.1288A>G
|
NP_001243586.1:p.Ile430Val
|
|