ENST00000369733.8:c.711C>G
|
ENSP00000358748.3:p.Asn237Lys
|
|
ENST00000648076.2:c.711C>G
MANE Select
|
ENSP00000497653.1:p.Asn237Lys
|
|
ENST00000649118.1:n.826C>G
|
|
|
ENST00000650263.1:c.663C>G
|
ENSP00000497850.1:p.Asn221Lys
|
|
ENST00000353479.9:c.711C>G
|
ENSP00000340937.5:p.Asn237Lys
|
|
ENST00000369733.7:c.711C>G
|
ENSP00000358748.3:p.Asn237Lys
|
|
ENST00000393211.3:c.711C>G
|
ENSP00000376905.3:p.Asn237Lys
|
|
ENST00000488320.1:n.56C>G
|
|
|
NM_000494.3:c.711C>G
|
NP_000485.3:p.Asn237Lys
|
|
NM_000494.4:c.711C>G
MANE Select
|
NP_000485.3:p.Asn237Lys
|
|