ENST00000262367.10:c.4541G>A
MANE Select
|
ENSP00000262367.5:p.Arg1514Gln
|
|
ENST00000262367.9:c.4541G>A
|
ENSP00000262367.5:p.Arg1514Gln
|
|
ENST00000382070.7:c.4427G>A
|
ENSP00000371502.3:p.Arg1476Gln
|
|
ENST00000570939.2:c.3176G>A
|
ENSP00000461002.2:p.Arg1059Gln
|
|
ENST00000571763.5:n.331G>A
|
|
|
ENST00000574740.1:n.362G>A
|
|
|
ENST00000576720.1:n.3364G>A
|
|
|
NM_001079846.1:c.4427G>A
|
NP_001073315.1:p.Arg1476Gln
|
|
NM_004380.2:c.4541G>A
|
NP_004371.2:p.Arg1514Gln
|
|
XM_005255124.3:c.4496G>A
|
XP_005255181.1:p.Arg1499Gln
|
|
XM_005255125.3:c.4124G>A
|
XP_005255182.1:p.Arg1375Gln
|
|
XM_006720848.2:c.4280G>A
|
XP_006720911.1:p.Arg1427Gln
|
|
XM_011522380.1:c.4487G>A
|
XP_011520682.1:p.Arg1496Gln
|
|
XM_011522381.1:c.3788G>A
|
XP_011520683.1:p.Arg1263Gln
|
|
XM_005255124.4:c.4496G>A
|
XP_005255181.1:p.Arg1499Gln
|
|
XM_005255125.4:c.4124G>A
|
XP_005255182.1:p.Arg1375Gln
|
|
XM_006720848.3:c.4280G>A
|
XP_006720911.1:p.Arg1427Gln
|
|
XM_011522381.2:c.3788G>A
|
XP_011520683.1:p.Arg1263Gln
|
|
XM_017022944.1:c.4535G>A
|
XP_016878433.1:p.Arg1512Gln
|
|
NM_004380.3:c.4541G>A
MANE Select
|
NP_004371.2:p.Arg1514Gln
|
|