ENST00000352909.8:c.946C>A
MANE Select
|
ENSP00000325951.4:p.His316Asn
|
|
ENST00000324155.8:c.*635C>A
|
ENSP00000325831.3:n.*635C>A
|
|
ENST00000333684.9:c.696-115C>A
|
ENSP00000328814.6:n.696-115C>A
|
|
ENST00000352909.7:c.946C>A
|
ENSP00000325951.3:p.His316Asn
|
|
ENST00000381168.7:c.*666C>A
|
ENSP00000370560.3:n.*666C>A
|
|
ENST00000381175.5:c.1027C>A
|
ENSP00000370567.1:p.His343Asn
|
|
ENST00000381178.5:c.1039C>A
|
ENSP00000370571.1:p.His347Asn
|
|
ENST00000412076.1:c.136-115C>A
|
|
|
ENST00000416223.5:c.240C>A
|
|
|
ENST00000461172.1:n.111C>A
|
|
|
ENST00000479437.5:n.495C>A
|
|
|
NM_000360.3:c.946C>A
|
NP_000351.2:p.His316Asn
|
|
NM_199292.2:c.1039C>A
|
NP_954986.2:p.His347Asn
|
|
NM_199293.2:c.1027C>A
|
NP_954987.2:p.His343Asn
|
|
XM_011520335.1:c.958C>A
|
XP_011518637.1:p.His320Asn
|
|
XM_011520335.2:c.958C>A
|
XP_011518637.1:p.His320Asn
|
|
NM_000360.4:c.946C>A
MANE Select
|
NP_000351.2:p.His316Asn
|
|
NM_199292.3:c.1039C>A
|
NP_954986.2:p.His347Asn
|
|
NM_199293.3:c.1027C>A
|
NP_954987.2:p.His343Asn
|
|