ENST00000682565.1:c.10168C>A
|
ENSP00000507671.1:p.His3390Asn
|
|
ENST00000682801.1:c.10168C>A
|
ENSP00000507862.1:p.His3390Asn
|
|
ENST00000682859.1:c.10168C>A
|
ENSP00000508222.1:p.His3390Asn
|
|
ENST00000683791.1:c.3254C>A
|
|
|
ENST00000684460.1:c.7449C>A
|
|
|
ENST00000684548.1:c.10168C>A
|
ENSP00000507421.1:p.His3390Asn
|
|
ENST00000684590.1:c.4615C>A
|
ENSP00000507376.1:p.His1539Asn
|
|
ENST00000684656.1:c.7494C>A
|
|
|
ENST00000613296.6:c.10549C>A
MANE Select
|
ENSP00000482968.1:p.His3517Asn
|
|
ENST00000651057.1:c.703C>A
|
ENSP00000498504.1:p.His235Asn
|
|
ENST00000651434.1:c.1905C>A
|
|
|
ENST00000652487.1:c.1646C>A
|
|
|
ENST00000423048.5:c.4040C>A
|
ENSP00000399833.1:n.4040C>A
|
|
ENST00000484298.5:c.10423C>A
|
ENSP00000478155.1:p.His3475Asn
|
|
ENST00000613296.4:c.10549C>A
|
ENSP00000482968.1:p.His3517Asn
|
|
ENST00000614410.4:c.10549C>A
|
ENSP00000479094.1:p.His3517Asn
|
|
ENST00000620466.4:n.4352C>A
|
|
|
NM_015120.4:c.10552C>A , LRG_741t1:c.10552C>A
|
NP_055935.4:p.His3518Asn
|
|
NM_001378454.1:c.10549C>A
MANE Select
|
NP_001365383.1:p.His3517Asn
|
|