ENST00000258385.8:c.1337T>A
MANE Select
|
ENSP00000258385.3:p.Val446Asp
|
|
ENST00000258385.7:c.1337T>A
|
ENSP00000258385.3:p.Val446Asp
|
|
ENST00000441621.6:c.*519T>A
|
ENSP00000408819.2:n.*519T>A
|
|
ENST00000446616.1:c.*978T>A
|
ENSP00000410801.1:n.*978T>A
|
|
ENST00000543200.5:c.1292T>A
|
ENSP00000438380.1:p.Val431Asp
|
|
NM_000751.2:c.1337T>A
|
NP_000742.1:p.Val446Asp
|
|
NM_001256657.1:c.1292T>A
|
NP_001243586.1:p.Val431Asp
|
|
NM_001311195.1:c.755T>A
|
NP_001298124.1:p.Val252Asp
|
|
NM_001311196.1:c.1034T>A
|
NP_001298125.1:p.Val345Asp
|
|
NR_046333.1:c.-4294966214T>A
|
|
|
NR_046334.1:c.-4294965935T>A
|
|
|
XM_011510524.1:c.956T>A
|
XP_011508826.1:p.Val319Asp
|
|
XM_011510524.2:c.956T>A
|
XP_011508826.1:p.Val319Asp
|
|
NM_000751.3:c.1337T>A
MANE Select
|
NP_000742.1:p.Val446Asp
|
|
NM_001311195.2:c.755T>A
|
NP_001298124.1:p.Val252Asp
|
|
NM_001311196.2:c.1034T>A
|
NP_001298125.1:p.Val345Asp
|
|
NM_001256657.2:c.1292T>A
|
NP_001243586.1:p.Val431Asp
|
|