ENST00000576204.6:n.905G>A
|
|
|
ENST00000622290.5:c.*214G>A
|
ENSP00000483331.2:n.*214G>A
|
|
ENST00000205557.12:c.4042G>A
MANE Select
|
ENSP00000205557.7:p.Asp1348Asn
|
|
ENST00000640696.1:c.856G>A
|
ENSP00000492197.1:p.Asp286Asn
|
|
ENST00000205557.11:c.4042G>A
|
ENSP00000205557.7:p.Asp1348Asn
|
|
ENST00000456970.6:c.3667G>A
|
ENSP00000405002.2:n.3667G>A
|
|
ENST00000576204.5:n.905G>A
|
|
|
ENST00000622290.4:c.*1251G>A
|
ENSP00000483331.1:n.*1251G>A
|
|
NM_001171.5:c.4042G>A
|
NP_001162.4:p.Asp1348Asn
|
|
XM_011522479.1:c.4009G>A
|
XP_011520781.1:p.Asp1337Asn
|
|
XM_011522480.1:c.3700G>A
|
XP_011520782.1:p.Asp1234Asn
|
|
XM_011522481.1:c.3700G>A
|
XP_011520783.1:p.Asp1234Asn
|
|
XR_933134.1:n.539-4987C>T
|
|
|
NM_001351800.1:c.3700G>A
|
NP_001338729.1:p.Asp1234Asn
|
|
NR_147784.1:n.3704G>A
|
|
|
XM_011522479.2:c.4009G>A
|
XP_011520781.1:p.Asp1337Asn
|
|
XM_011522481.3:c.3700G>A
|
XP_011520783.1:p.Asp1234Asn
|
|
XM_017023212.1:c.3874G>A
|
XP_016878701.1:p.Asp1292Asn
|
|
XM_024450261.1:c.4078G>A
|
XP_024306029.1:p.Asp1360Asn
|
|
NM_001171.6:c.4042G>A
MANE Select
|
NP_001162.5:p.Asp1348Asn
|
|