ENST00000494707.6:c.425A>G
|
|
|
ENST00000642170.1:n.1475A>G
|
|
|
ENST00000642395.2:c.1221A>G
|
ENSP00000493468.2:p.Ser407=
|
|
ENST00000642558.1:c.1128A>G
|
ENSP00000496427.1:p.Ser376=
|
|
ENST00000642739.1:c.1221A>G
|
ENSP00000493596.1:p.Ser407=
|
|
ENST00000644238.1:c.1060-1528A>G
|
ENSP00000496728.1:n.1060-1528A>G
|
|
ENST00000644337.1:c.1060-1528A>G
|
ENSP00000494557.1:n.1060-1528A>G
|
|
ENST00000645032.1:c.1221A>G
MANE Select
|
ENSP00000495537.1:p.Ser407=
|
|
ENST00000645124.1:c.1221A>G
|
ENSP00000496446.1:p.Ser407=
|
|
ENST00000646020.1:c.1281A>G
|
ENSP00000494745.1:p.Ser427=
|
|
ENST00000318842.11:c.1221A>G
|
ENSP00000322219.6:p.Ser407=
|
|
ENST00000339363.7:c.1221A>G
|
ENSP00000343671.3:p.Ser407=
|
|
ENST00000378505.6:c.1221A>G
|
ENSP00000367766.2:p.Ser407=
|
|
ENST00000464437.1:c.287A>G
|
|
|
ENST00000465127.1:c.172-367141T>C
|
ENSP00000417050.1:n.172-367141T>C
|
|
ENST00000474584.5:c.1221A>G
|
ENSP00000418926.1:p.Ser407=
|
|
ENST00000482855.5:c.1221A>G
|
ENSP00000419276.1:p.Ser407=
|
|
ENST00000494841.1:n.484A>G
|
|
|
NM_000328.2:c.1221A>G
|
NP_000319.1:p.Ser407=
|
|
NM_001034853.1:c.1221A>G
|
NP_001030025.1:p.Ser407=
|
|
XM_005272633.1:c.1221A>G
|
XP_005272690.1:p.Ser407=
|
|
XM_011543940.1:c.1218A>G
|
XP_011542242.1:p.Ser406=
|
|
XM_005272633.3:c.1221A>G
|
XP_005272690.1:p.Ser407=
|
|
XM_011543940.3:c.1218A>G
|
XP_011542242.1:p.Ser406=
|
|
XM_017029712.2:c.1218A>G
|
XP_016885201.1:p.Ser406=
|
|
NM_001367245.1:c.1218A>G
|
NP_001354174.1:p.Ser406=
|
|
NM_001367246.1:c.1060-1528A>G
|
NP_001354175.1:n.1060-1528A>G
|
|
NM_001367247.1:c.1221A>G
|
NP_001354176.1:p.Ser407=
|
|
NM_001367248.1:c.1251A>G
|
NP_001354177.1:p.Ser417=
|
|
NM_001367249.1:c.1218A>G
|
NP_001354178.1:p.Ser406=
|
|
NM_001367250.1:c.1218A>G
|
NP_001354179.1:p.Ser406=
|
|
NM_001367251.1:c.1060-1528A>G
|
NP_001354180.1:n.1060-1528A>G
|
|
NR_159803.1:n.1423A>G
|
|
|
NR_159804.1:n.1272A>G
|
|
|
NR_159805.1:n.1363A>G
|
|
|
NR_159806.1:n.1363A>G
|
|
|
NR_159807.1:n.1363A>G
|
|
|
NR_159808.1:n.1475A>G
|
|
|
NM_000328.3:c.1221A>G
|
NP_000319.1:p.Ser407=
|
|
NM_001034853.2:c.1221A>G
MANE Select
|
NP_001030025.1:p.Ser407=
|
|