ENST00000205402.10:c.825T>G
MANE Select
|
ENSP00000205402.3:p.Asn275Lys
|
|
ENST00000205402.9:c.825T>G
|
ENSP00000205402.3:p.Asn275Lys
|
|
ENST00000415325.5:c.*499T>G
|
ENSP00000402593.1:n.*499T>G
|
|
ENST00000417551.5:c.825T>G
|
ENSP00000390667.1:p.Asn275Lys
|
|
ENST00000437604.6:c.681T>G
|
ENSP00000387542.2:p.Asn227Lys
|
|
ENST00000440410.5:c.756T>G
|
ENSP00000417016.1:p.Asn252Lys
|
|
NM_000108.4:c.825T>G
|
NP_000099.2:p.Asn275Lys
|
|
NM_001289750.1:c.528T>G
|
NP_001276679.1:p.Asn176Lys
|
|
NM_001289751.1:c.756T>G
|
NP_001276680.1:p.Asn252Lys
|
|
NM_001289752.1:c.681T>G
|
NP_001276681.1:p.Asn227Lys
|
|
NM_000108.5:c.825T>G
MANE Select
|
NP_000099.2:p.Asn275Lys
|
|