ENST00000529510.6:n.993A>T
|
|
|
ENST00000697845.1:n.917A>T
|
|
|
ENST00000697846.1:n.993A>T
|
|
|
ENST00000697847.1:n.993A>T
|
|
|
ENST00000697848.1:n.993A>T
|
|
|
ENST00000697849.1:n.2032A>T
|
|
|
ENST00000697850.1:n.993A>T
|
|
|
ENST00000697851.1:n.2353A>T
|
|
|
ENST00000638186.1:n.1067A>T
|
|
|
ENST00000638360.1:n.899A>T
|
|
|
ENST00000638925.1:n.1000A>T
|
|
|
ENST00000650539.1:n.1169A>T
|
|
|
ENST00000330775.9:c.763A>T
|
ENSP00000476242.2:p.Lys255Ter
|
|
ENST00000357590.9:c.763A>T
|
ENSP00000476176.2:p.Lys255Ter
|
|
ENST00000524428.5:n.1085A>T
|
|
|
ENST00000525039.5:n.1187A>T
|
|
|
ENST00000525102.5:n.1521A>T
|
|
|
ENST00000525372.5:n.764A>T
|
|
|
ENST00000526275.5:n.1545A>T
|
|
|
ENST00000526626.6:n.726A>T
|
|
|
ENST00000527992.5:n.991A>T
|
|
|
ENST00000529510.5:n.537A>T
|
|
|
ENST00000530407.5:n.913A>T
|
|
|
ENST00000532085.1:n.3374A>T
|
|
|
ENST00000532888.6:n.1059A>T
|
|
|
ENST00000538950.5:c.544A>T
|
ENSP00000475991.2:p.Lys182Ter
|
|
ENST00000545985.5:c.763A>T
|
ENSP00000475241.2:p.Lys255Ter
|
|
NM_001164277.1:c.763A>T , LRG_187t1:c.763A>T
|
NP_001157749.1:p.Lys255Ter
|
|
NM_001164278.1:c.763A>T
|
NP_001157750.1:p.Lys255Ter
|
|
NM_001164279.1:c.544A>T
|
NP_001157751.1:p.Lys182Ter
|
|
NM_001164280.1:c.763A>T
|
NP_001157752.1:p.Lys255Ter
|
|
NM_001467.5:c.763A>T
|
NP_001458.1:p.Lys255Ter
|
|
NM_001164278.2:c.763A>T
|
NP_001157750.1:p.Lys255Ter
|
|
NM_001164279.2:c.544A>T
|
NP_001157751.1:p.Lys182Ter
|
|
NM_001164280.2:c.763A>T
|
NP_001157752.1:p.Lys255Ter
|
|
NM_001467.6:c.763A>T
|
NP_001458.1:p.Lys255Ter
|
|
NM_001164277.2:c.763A>T
MANE Select
|
NP_001157749.1:p.Lys255Ter
|
|