ENST00000258385.8:c.299T>G
MANE Select
|
ENSP00000258385.3:p.Val100Gly
|
|
ENST00000258385.7:c.299T>G
|
ENSP00000258385.3:p.Val100Gly
|
|
ENST00000412233.5:c.299T>G
|
ENSP00000398143.1:p.Val100Gly
|
|
ENST00000441621.6:c.299T>G
|
ENSP00000408819.2:p.Val100Gly
|
|
ENST00000446616.1:c.299T>G
|
ENSP00000410801.1:p.Val100Gly
|
|
ENST00000449596.5:c.254T>G
|
ENSP00000404950.1:p.Val85Gly
|
|
ENST00000543200.5:c.254T>G
|
ENSP00000438380.1:p.Val85Gly
|
|
NM_000751.2:c.299T>G
|
NP_000742.1:p.Val100Gly
|
|
NM_001256657.1:c.254T>G
|
NP_001243586.1:p.Val85Gly
|
|
NM_001311195.1:c.28T>G
|
NP_001298124.1:p.Ser10Ala
|
|
NM_001311196.1:c.28T>G
|
NP_001298125.1:p.Ser10Ala
|
|
NR_046333.1:c.-4294966941T>G
|
|
|
NR_046334.1:c.-4294966941T>G
|
|
|
XM_011510524.1:c.28T>G
|
XP_011508826.1:p.Ser10Ala
|
|
XM_011510524.2:c.28T>G
|
XP_011508826.1:p.Ser10Ala
|
|
NM_000751.3:c.299T>G
MANE Select
|
NP_000742.1:p.Val100Gly
|
|
NM_001311195.2:c.28T>G
|
NP_001298124.1:p.Ser10Ala
|
|
NM_001311196.2:c.28T>G
|
NP_001298125.1:p.Ser10Ala
|
|
NM_001256657.2:c.254T>G
|
NP_001243586.1:p.Val85Gly
|
|