ENST00000642683.1:c.723A>C
|
ENSP00000495376.1:p.Gln241His
|
|
ENST00000643672.1:c.720A>C
|
ENSP00000494532.1:p.Gln240His
|
|
ENST00000645280.1:c.717A>C
|
ENSP00000496690.1:p.Gln239His
|
|
ENST00000648579.1:c.*68A>C
|
ENSP00000497638.1:n.*68A>C
|
|
ENST00000650617.1:c.771A>C
MANE Select
|
ENSP00000497532.1:p.Gln257His
|
|
ENST00000273158.8:c.771A>C
|
ENSP00000273158.3:p.Gln257His
|
|
NM_017875.2:c.771A>C
|
NP_060345.2:p.Gln257His
|
|
XM_006713214.1:c.759A>C
|
XP_006713277.1:p.Gln253His
|
|
XM_011533869.1:c.753A>C
|
XP_011532171.1:p.Gln251His
|
|
XM_011533870.1:c.720A>C
|
XP_011532172.1:p.Gln240His
|
|
XM_011533871.1:c.591A>C
|
XP_011532173.1:p.Gln197His
|
|
NM_001354798.1:c.626-1843A>C
|
NP_001341727.1:n.626-1843A>C
|
|
NM_017875.4:c.771A>C
MANE Select
|
NP_060345.2:p.Gln257His
|
|
XM_006713214.2:c.759A>C
|
XP_006713277.1:p.Gln253His
|
|
XM_011533869.2:c.753A>C
|
XP_011532171.1:p.Gln251His
|
|
XM_024453611.1:c.717A>C
|
XP_024309379.1:p.Gln239His
|
|
NM_001354798.2:c.626-1843A>C
|
NP_001341727.1:n.626-1843A>C
|
|