ENST00000399820.8:c.3814A>C
MANE Select
|
ENSP00000382717.3:p.Asn1272His
|
|
ENST00000399820.7:c.3814A>C
|
ENSP00000382717.3:p.Asn1272His
|
|
ENST00000503733.1:n.154A>C
|
|
|
ENST00000506869.5:c.*3395A>C
|
ENSP00000424319.1:n.*3395A>C
|
|
ENST00000512534.5:n.2125A>C
|
|
|
ENST00000512588.5:n.156A>C
|
|
|
NM_025132.3:c.3814A>C
|
NP_079408.3:p.Asn1272His
|
|
XM_011513724.1:c.3826A>C
|
XP_011512026.1:p.Asn1276His
|
|
XM_011513725.1:c.3760A>C
|
XP_011512027.1:p.Asn1254His
|
|
XM_011513726.1:c.3346A>C
|
XP_011512028.1:p.Asn1116His
|
|
XM_011513727.1:c.3346A>C
|
XP_011512029.1:p.Asn1116His
|
|
XM_011513728.1:c.3334A>C
|
XP_011512030.1:p.Asn1112His
|
|
XR_925155.1:n.5524A>C
|
|
|
NM_001317924.1:c.3334A>C
|
NP_001304853.1:p.Asn1112His
|
|
XM_011513725.2:c.3760A>C
|
XP_011512027.1:p.Asn1254His
|
|
XM_011513726.3:c.3346A>C
|
XP_011512028.1:p.Asn1116His
|
|
XM_017008501.1:c.3334A>C
|
XP_016863990.1:p.Asn1112His
|
|
XR_001741306.1:n.4091A>C
|
|
|
XR_001741307.1:n.4079A>C
|
|
|
XR_001741308.1:n.5725A>C
|
|
|
XR_001741309.1:n.5512A>C
|
|
|
XR_001741310.1:n.5713A>C
|
|
|
XR_001741311.2:n.5361A>C
|
|
|
NM_025132.4:c.3814A>C
MANE Select
|
NP_079408.3:p.Asn1272His
|
|
NM_001317924.2:c.3334A>C
|
NP_001304853.1:p.Asn1112His
|
|