ENST00000371757.7:c.3560A>G
MANE Select
|
ENSP00000360822.2:p.Asp1187Gly
|
|
ENST00000674572.1:c.3464A>G
|
ENSP00000501742.1:p.Asp1155Gly
|
|
ENST00000675090.1:c.3308A>G
|
ENSP00000501833.1:p.Asp1103Gly
|
|
ENST00000675399.1:c.3371A>G
|
ENSP00000501932.1:p.Asp1124Gly
|
|
ENST00000676421.1:c.3380A>G
|
ENSP00000502322.1:p.Asp1127Gly
|
|
ENST00000263604.5:c.3524A>G
|
ENSP00000263604.4:p.Asp1175Gly
|
|
ENST00000371757.6:c.3560A>G
|
ENSP00000360822.2:p.Asp1187Gly
|
|
ENST00000460750.5:c.*3233A>G
|
ENSP00000418777.1:n.*3233A>G
|
|
ENST00000475008.1:n.2866A>G
|
|
|
ENST00000486577.6:c.3506A>G
|
ENSP00000417578.3:p.Asp1169Gly
|
|
ENST00000487664.5:c.3623A>G
|
ENSP00000417851.2:p.Asp1208Gly
|
|
ENST00000488444.6:c.3545A>G
|
ENSP00000419007.3:p.Asp1182Gly
|
|
ENST00000490355.6:c.3560A>G
|
ENSP00000418003.3:p.Asp1187Gly
|
|
ENST00000491806.6:c.3503A>G
|
ENSP00000419086.3:p.Asp1168Gly
|
|
ENST00000628528.2:c.3488A>G
|
ENSP00000486374.1:p.Asp1163Gly
|
|
ENST00000630792.2:c.3458A>G
|
ENSP00000486486.1:p.Asp1153Gly
|
|
ENST00000631073.2:c.3566A>G
|
ENSP00000486130.1:p.Asp1189Gly
|
|
NM_001272003.1:c.3488A>G
|
NP_001258932.1:p.Asp1163Gly
|
|
NM_020822.2:c.3560A>G
|
NP_065873.2:p.Asp1187Gly
|
|
XM_011518877.1:c.3758A>G
|
XP_011517179.1:p.Asp1253Gly
|
|
XM_011518878.1:c.3704A>G
|
XP_011517180.1:p.Asp1235Gly
|
|
XM_011518879.1:c.3695A>G
|
XP_011517181.1:p.Asp1232Gly
|
|
XM_011518880.1:c.3524A>G
|
XP_011517182.1:p.Asp1175Gly
|
|
XM_011518881.1:c.3113A>G
|
XP_011517183.1:p.Asp1038Gly
|
|
XM_011518877.3:c.3758A>G
|
XP_011517179.1:p.Asp1253Gly
|
|
XM_011518878.3:c.3704A>G
|
XP_011517180.1:p.Asp1235Gly
|
|
XM_011518879.3:c.3695A>G
|
XP_011517181.1:p.Asp1232Gly
|
|
XM_011518881.3:c.3113A>G
|
XP_011517183.1:p.Asp1038Gly
|
|
XM_017014931.1:c.3557A>G
|
XP_016870420.1:p.Asp1186Gly
|
|
XM_017014932.1:c.3380A>G
|
XP_016870421.1:p.Asp1127Gly
|
|
XM_017014933.1:c.3113A>G
|
XP_016870422.1:p.Asp1038Gly
|
|
XM_024447617.1:c.3113A>G
|
XP_024303385.1:p.Asp1038Gly
|
|
XM_024447618.1:c.3113A>G
|
XP_024303386.1:p.Asp1038Gly
|
|
NM_020822.3:c.3560A>G
MANE Select
|
NP_065873.2:p.Asp1187Gly
|
|
NM_001272003.2:c.3488A>G
|
NP_001258932.1:p.Asp1163Gly
|
|