ENST00000281928.9:c.5584A>C
MANE Select
|
ENSP00000281928.3:p.Asn1862His
|
|
ENST00000548694.2:n.373A>C
|
|
|
ENST00000648379.1:n.3952A>C
|
|
|
ENST00000648737.1:n.5348A>C
|
|
|
ENST00000648825.1:n.3769A>C
|
|
|
ENST00000648916.1:n.3595A>C
|
|
|
ENST00000649607.1:c.3768A>C
|
|
|
ENST00000649775.1:c.2073A>C
|
|
|
ENST00000650226.1:c.5584A>C
|
ENSP00000496981.1:p.Asn1862His
|
|
ENST00000281928.7:c.5584A>C
|
ENSP00000281928.3:p.Asn1862His
|
|
ENST00000548694.1:n.373A>C
|
|
|
ENST00000552447.1:c.161A>C
|
|
|
NM_015335.4:c.5584A>C
|
NP_056150.1:p.Asn1862His
|
|
XM_011538080.1:c.5584A>C
|
XP_011536382.1:p.Asn1862His
|
|
XM_011538081.1:c.5581A>C
|
XP_011536383.1:p.Asn1861His
|
|
XM_011538082.1:c.5554A>C
|
XP_011536384.1:p.Asn1852His
|
|
XM_011538080.2:c.5584A>C
|
XP_011536382.1:p.Asn1862His
|
|
XM_011538081.2:c.5581A>C
|
XP_011536383.1:p.Asn1861His
|
|
XM_011538082.2:c.5554A>C
|
XP_011536384.1:p.Asn1852His
|
|
XM_017019090.1:c.5581A>C
|
XP_016874579.1:p.Asn1861His
|
|
NM_015335.5:c.5584A>C
MANE Select
|
NP_056150.1:p.Asn1862His
|
|