ENST00000262367.10:c.3988C>T
MANE Select
|
ENSP00000262367.5:p.Gln1330Ter
|
|
ENST00000262367.9:c.3988C>T
|
ENSP00000262367.5:p.Gln1330Ter
|
|
ENST00000382070.7:c.3874C>T
|
ENSP00000371502.3:p.Gln1292Ter
|
|
ENST00000570939.2:c.2623C>T
|
ENSP00000461002.2:p.Gln875Ter
|
|
ENST00000572569.1:n.452C>T
|
|
|
ENST00000573517.6:c.294C>T
|
|
|
ENST00000574740.1:n.70C>T
|
|
|
ENST00000576720.1:n.2925C>T
|
|
|
NM_001079846.1:c.3874C>T
|
NP_001073315.1:p.Gln1292Ter
|
|
NM_004380.2:c.3988C>T
|
NP_004371.2:p.Gln1330Ter
|
|
XM_005255124.3:c.3943C>T
|
XP_005255181.1:p.Gln1315Ter
|
|
XM_005255125.3:c.3571C>T
|
XP_005255182.1:p.Gln1191Ter
|
|
XM_006720848.2:c.3988C>T
|
XP_006720911.1:p.Gln1330Ter
|
|
XM_011522380.1:c.3934C>T
|
XP_011520682.1:p.Gln1312Ter
|
|
XM_011522381.1:c.3235C>T
|
XP_011520683.1:p.Gln1079Ter
|
|
XM_005255124.4:c.3943C>T
|
XP_005255181.1:p.Gln1315Ter
|
|
XM_005255125.4:c.3571C>T
|
XP_005255182.1:p.Gln1191Ter
|
|
XM_006720848.3:c.3988C>T
|
XP_006720911.1:p.Gln1330Ter
|
|
XM_011522381.2:c.3235C>T
|
XP_011520683.1:p.Gln1079Ter
|
|
XM_017022944.1:c.3982C>T
|
XP_016878433.1:p.Gln1328Ter
|
|
NM_004380.3:c.3988C>T
MANE Select
|
NP_004371.2:p.Gln1330Ter
|
|