ENST00000650516.2:c.1612C>A
|
ENSP00000498052.2:p.His538Asn
|
|
ENST00000343257.7:c.1612C>A
MANE Select
|
ENSP00000339867.2:p.His538Asn
|
|
ENST00000432192.6:c.1436C>A
|
|
|
ENST00000343257.6:c.1612C>A
|
ENSP00000339867.2:p.His538Asn
|
|
NM_000083.2:c.1612C>A
|
NP_000074.2:p.His538Asn
|
|
NR_046453.1:n.1552C>A
|
|
|
XM_011515781.1:c.1636C>A
|
XP_011514083.1:p.His546Asn
|
|
XM_011515782.1:c.358C>A
|
XP_011514084.1:p.His120Asn
|
|
XM_011515782.2:c.358C>A
|
XP_011514084.1:p.His120Asn
|
|
XM_017011739.1:c.1186C>A
|
XP_016867228.1:p.His396Asn
|
|
XM_017011740.1:c.1162C>A
|
XP_016867229.1:p.His388Asn
|
|
NM_000083.3:c.1612C>A
MANE Select
|
NP_000074.3:p.His538Asn
|
|
NR_046453.2:n.1567C>A
|
|
|