ENST00000703783.1:n.533A>G
|
|
|
ENST00000703785.1:n.614A>G
|
|
|
ENST00000262464.9:c.3749A>G
MANE Select
|
ENSP00000262464.4:p.Asn1250Ser
|
|
ENST00000262464.8:c.3749A>G
|
ENSP00000262464.4:p.Asn1250Ser
|
|
ENST00000507835.5:c.299A>G
|
ENSP00000426839.1:p.Asn100Ser
|
|
ENST00000508053.5:c.3749A>G
|
ENSP00000424571.1:p.Asn1250Ser
|
|
ENST00000508989.5:c.3650A>G
|
ENSP00000425596.1:p.Asn1217Ser
|
|
ENST00000619499.4:c.3746A>G
|
ENSP00000482132.1:p.Asn1249Ser
|
|
NM_001999.3:c.3749A>G
|
NP_001990.2:p.Asn1250Ser
|
|
XM_017009228.2:c.3596A>G
|
XP_016864717.1:p.Asn1199Ser
|
|
NM_001999.4:c.3749A>G
MANE Select
|
NP_001990.2:p.Asn1250Ser
|
|