ENST00000247933.9:c.1243A>G
|
ENSP00000247933.4:p.Asn415Asp
|
|
ENST00000514224.2:c.1243A>G
MANE Select
|
ENSP00000425081.2:p.Asn415Asp
|
|
ENST00000652070.1:n.1299A>G
|
|
|
ENST00000247933.8:c.1243A>G
|
ENSP00000247933.4:p.Asn415Asp
|
|
ENST00000502829.1:n.45A>G
|
|
|
ENST00000514224.1:c.847A>G
|
ENSP00000425081.1:p.Asn283Asp
|
|
ENST00000514698.5:n.1350A>G
|
|
|
NM_000203.4:c.1243A>G
|
NP_000194.2:p.Asn415Asp
|
|
NR_110313.1:n.1331A>G
|
|
|
XM_006713882.2:c.847A>G
|
XP_006713945.1:p.Asn283Asp
|
|
XM_011513459.1:c.1309A>G
|
XP_011511761.1:p.Asn437Asp
|
|
XM_011513460.1:c.1102A>G
|
XP_011511762.1:p.Asn368Asp
|
|
XM_011513461.1:c.1036A>G
|
XP_011511763.1:p.Asn346Asp
|
|
XM_011513462.1:c.955A>G
|
XP_011511764.1:p.Asn319Asp
|
|
XM_011513463.1:c.955A>G
|
XP_011511765.1:p.Asn319Asp
|
|
XR_924947.1:n.1312A>G
|
|
|
NM_000203.5:c.1243A>G
MANE Select
|
NP_000194.2:p.Asn415Asp
|
|
NM_001363576.1:c.847A>G
|
NP_001350505.1:p.Asn283Asp
|
|
XM_011513461.2:c.1036A>G
|
XP_011511763.1:p.Asn346Asp
|
|
XM_017008163.1:c.283A>G
|
XP_016863652.1:p.Asn95Asp
|
|