ENST00000262367.10:c.4430G>A
MANE Select
|
ENSP00000262367.5:p.Ser1477Asn
|
|
ENST00000262367.9:c.4430G>A
|
ENSP00000262367.5:p.Ser1477Asn
|
|
ENST00000382070.7:c.4316G>A
|
ENSP00000371502.3:p.Ser1439Asn
|
|
ENST00000570939.2:c.3065G>A
|
ENSP00000461002.2:p.Ser1022Asn
|
|
ENST00000571763.5:n.220G>A
|
|
|
ENST00000574740.1:n.251G>A
|
|
|
ENST00000576720.1:n.3253G>A
|
|
|
NM_001079846.1:c.4316G>A
|
NP_001073315.1:p.Ser1439Asn
|
|
NM_004380.2:c.4430G>A
|
NP_004371.2:p.Ser1477Asn
|
|
XM_005255124.3:c.4385G>A
|
XP_005255181.1:p.Ser1462Asn
|
|
XM_005255125.3:c.4013G>A
|
XP_005255182.1:p.Ser1338Asn
|
|
XM_006720848.2:c.4169G>A
|
XP_006720911.1:p.Ser1390Asn
|
|
XM_011522380.1:c.4376G>A
|
XP_011520682.1:p.Ser1459Asn
|
|
XM_011522381.1:c.3677G>A
|
XP_011520683.1:p.Ser1226Asn
|
|
XM_005255124.4:c.4385G>A
|
XP_005255181.1:p.Ser1462Asn
|
|
XM_005255125.4:c.4013G>A
|
XP_005255182.1:p.Ser1338Asn
|
|
XM_006720848.3:c.4169G>A
|
XP_006720911.1:p.Ser1390Asn
|
|
XM_011522381.2:c.3677G>A
|
XP_011520683.1:p.Ser1226Asn
|
|
XM_017022944.1:c.4424G>A
|
XP_016878433.1:p.Ser1475Asn
|
|
NM_004380.3:c.4430G>A
MANE Select
|
NP_004371.2:p.Ser1477Asn
|
|