ENST00000622290.5:c.3712G>A
|
ENSP00000483331.2:p.Asp1238Asn
|
|
ENST00000205557.12:c.3712G>A
MANE Select
|
ENSP00000205557.7:p.Asp1238Asn
|
|
ENST00000640696.1:c.526G>A
|
ENSP00000492197.1:p.Asp176Asn
|
|
ENST00000205557.11:c.3712G>A
|
ENSP00000205557.7:p.Asp1238Asn
|
|
ENST00000456970.6:c.3337G>A
|
ENSP00000405002.2:n.3337G>A
|
|
ENST00000622290.4:c.*921G>A
|
ENSP00000483331.1:n.*921G>A
|
|
NM_001171.5:c.3712G>A
|
NP_001162.4:p.Asp1238Asn
|
|
XM_011522479.1:c.3679G>A
|
XP_011520781.1:p.Asp1227Asn
|
|
XM_011522480.1:c.3370G>A
|
XP_011520782.1:p.Asp1124Asn
|
|
XM_011522481.1:c.3370G>A
|
XP_011520783.1:p.Asp1124Asn
|
|
XR_932836.1:n.3947G>A
|
|
|
XR_932837.1:n.3748G>A
|
|
|
XR_932838.1:n.3748G>A
|
|
|
XR_933134.1:n.539-276C>T
|
|
|
NM_001351800.1:c.3370G>A
|
NP_001338729.1:p.Asp1124Asn
|
|
NR_147784.1:n.3374G>A
|
|
|
XM_011522479.2:c.3679G>A
|
XP_011520781.1:p.Asp1227Asn
|
|
XM_011522481.3:c.3370G>A
|
XP_011520783.1:p.Asp1124Asn
|
|
XM_017023212.1:c.3544G>A
|
XP_016878701.1:p.Asp1182Asn
|
|
XM_024450261.1:c.3748G>A
|
XP_024306029.1:p.Asp1250Asn
|
|
XR_932836.2:n.3893G>A
|
|
|
XR_932837.3:n.3693G>A
|
|
|
XR_932838.3:n.3693G>A
|
|
|
NM_001171.6:c.3712G>A
MANE Select
|
NP_001162.5:p.Asp1238Asn
|
|