ENST00000642683.1:c.681T>G
|
ENSP00000495376.1:p.Thr227=
|
|
ENST00000643672.1:c.678T>G
|
ENSP00000494532.1:p.Thr226=
|
|
ENST00000645280.1:c.675T>G
|
ENSP00000496690.1:p.Thr225=
|
|
ENST00000648579.1:c.*26T>G
|
ENSP00000497638.1:n.*26T>G
|
|
ENST00000650617.1:c.729T>G
MANE Select
|
ENSP00000497532.1:p.Thr243=
|
|
ENST00000273158.8:c.729T>G
|
ENSP00000273158.3:p.Thr243=
|
|
NM_017875.2:c.729T>G
|
NP_060345.2:p.Thr243=
|
|
XM_006713214.1:c.717T>G
|
XP_006713277.1:p.Thr239=
|
|
XM_011533869.1:c.711T>G
|
XP_011532171.1:p.Thr237=
|
|
XM_011533870.1:c.678T>G
|
XP_011532172.1:p.Thr226=
|
|
XM_011533871.1:c.549T>G
|
XP_011532173.1:p.Thr183=
|
|
NM_001354798.1:c.626-1885T>G
|
NP_001341727.1:n.626-1885T>G
|
|
NM_017875.4:c.729T>G
MANE Select
|
NP_060345.2:p.Thr243=
|
|
XM_006713214.2:c.717T>G
|
XP_006713277.1:p.Thr239=
|
|
XM_011533869.2:c.711T>G
|
XP_011532171.1:p.Thr237=
|
|
XM_024453611.1:c.675T>G
|
XP_024309379.1:p.Thr225=
|
|
NM_001354798.2:c.626-1885T>G
|
NP_001341727.1:n.626-1885T>G
|
|