ENST00000262093.11:c.1265A>G
MANE Select
|
ENSP00000262093.6:p.Gln422Arg
|
|
ENST00000382873.8:c.1049A>G
|
ENSP00000372326.4:p.Gln350Arg
|
|
ENST00000651787.1:n.1371A>G
|
|
|
ENST00000652755.1:c.1283A>G
|
ENSP00000498358.1:p.Gln428Arg
|
|
ENST00000262093.9:c.1265A>G
|
ENSP00000262093.5:p.Gln422Arg
|
|
ENST00000382873.7:c.1283A>G
|
ENSP00000372326.3:p.Gln428Arg
|
|
ENST00000585494.5:c.*992A>G
|
ENSP00000465243.1:n.*992A>G
|
|
NM_000140.3:c.1265A>G
|
NP_000131.2:p.Gln422Arg
|
|
NM_001012515.2:c.1283A>G
|
NP_001012533.1:p.Gln428Arg
|
|
XM_011525881.1:c.1184A>G
|
XP_011524183.1:p.Gln395Arg
|
|
XM_011525882.1:c.1049A>G
|
XP_011524184.1:p.Gln350Arg
|
|
NM_000140.4:c.1265A>G
|
NP_000131.2:p.Gln422Arg
|
|
NM_001012515.3:c.1283A>G
|
NP_001012533.1:p.Gln428Arg
|
|
XM_011525882.2:c.1049A>G
|
XP_011524184.1:p.Gln350Arg
|
|
XM_017025614.2:c.1166A>G
|
XP_016881103.1:p.Gln389Arg
|
|
NM_000140.5:c.1265A>G
MANE Select
|
NP_000131.2:p.Gln422Arg
|
|
NM_001012515.4:c.1283A>G
|
NP_001012533.1:p.Gln428Arg
|
|
NM_001371094.1:c.1166A>G
|
NP_001358023.1:p.Gln389Arg
|
|
NM_001371095.1:c.1049A>G
|
NP_001358024.1:p.Gln350Arg
|
|
NM_001374778.1:c.1205A>G
|
NP_001361707.1:p.Gln402Arg
|
|