ENST00000642683.1:c.726A>G
|
ENSP00000495376.1:p.Ala242=
|
|
ENST00000643672.1:c.723A>G
|
ENSP00000494532.1:p.Ala241=
|
|
ENST00000645280.1:c.720A>G
|
ENSP00000496690.1:p.Ala240=
|
|
ENST00000648579.1:c.*71A>G
|
ENSP00000497638.1:n.*71A>G
|
|
ENST00000650617.1:c.774A>G
MANE Select
|
ENSP00000497532.1:p.Ala258=
|
|
ENST00000273158.8:c.774A>G
|
ENSP00000273158.3:p.Ala258=
|
|
NM_017875.2:c.774A>G
|
NP_060345.2:p.Ala258=
|
|
XM_006713214.1:c.762A>G
|
XP_006713277.1:p.Ala254=
|
|
XM_011533869.1:c.756A>G
|
XP_011532171.1:p.Ala252=
|
|
XM_011533870.1:c.723A>G
|
XP_011532172.1:p.Ala241=
|
|
XM_011533871.1:c.594A>G
|
XP_011532173.1:p.Ala198=
|
|
NM_001354798.1:c.626-1840A>G
|
NP_001341727.1:n.626-1840A>G
|
|
NM_017875.4:c.774A>G
MANE Select
|
NP_060345.2:p.Ala258=
|
|
XM_006713214.2:c.762A>G
|
XP_006713277.1:p.Ala254=
|
|
XM_011533869.2:c.756A>G
|
XP_011532171.1:p.Ala252=
|
|
XM_024453611.1:c.720A>G
|
XP_024309379.1:p.Ala240=
|
|
NM_001354798.2:c.626-1840A>G
|
NP_001341727.1:n.626-1840A>G
|
|