ENST00000529510.6:n.1022T=
|
|
|
ENST00000697845.1:n.1802T=
|
|
|
ENST00000697846.1:n.1022T=
|
|
|
ENST00000697847.1:n.1202-316T=
|
|
|
ENST00000697848.1:n.1108T=
|
|
|
ENST00000697849.1:n.2917T=
|
|
|
ENST00000697850.1:n.1108T=
|
|
|
ENST00000697851.1:n.2716T=
|
|
|
ENST00000638186.1:n.1182T=
|
|
|
ENST00000638360.1:n.1014T=
|
|
|
ENST00000638925.1:n.1147T=
|
|
|
ENST00000650539.1:n.1284T=
|
|
|
ENST00000330775.9:c.878T=
|
ENSP00000476242.2:p.Leu293=
|
|
ENST00000357590.9:c.878T=
|
ENSP00000476176.2:p.Leu293=
|
|
ENST00000524428.5:n.1114T=
|
|
|
ENST00000525039.5:n.1302T=
|
|
|
ENST00000525102.5:n.1636T=
|
|
|
ENST00000525372.5:n.976T=
|
|
|
ENST00000526275.5:n.1660T=
|
|
|
ENST00000527992.5:n.1106T=
|
|
|
ENST00000529510.5:n.566T=
|
|
|
ENST00000530407.5:n.1028T=
|
|
|
ENST00000532085.1:n.4259T=
|
|
|
ENST00000538950.5:c.659T=
|
ENSP00000475991.2:p.Leu220=
|
|
ENST00000545985.5:c.878T=
|
ENSP00000475241.2:p.Leu293=
|
|
NM_001164277.1:c.878T= , LRG_187t1:c.878T=
|
NP_001157749.1:p.Leu293=
|
|
NM_001164278.1:c.878T=
|
NP_001157750.1:p.Leu293=
|
|
NM_001164279.1:c.659T=
|
NP_001157751.1:p.Leu220=
|
|
NM_001164280.1:c.878T=
|
NP_001157752.1:p.Leu293=
|
|
NM_001467.5:c.878T=
|
NP_001458.1:p.Leu293=
|
|
NM_001164278.2:c.878T=
|
NP_001157750.1:p.Leu293=
|
|
NM_001164279.2:c.659T=
|
NP_001157751.1:p.Leu220=
|
|
NM_001164280.2:c.878T=
|
NP_001157752.1:p.Leu293=
|
|
NM_001467.6:c.878T=
|
NP_001458.1:p.Leu293=
|
|
NM_001164277.2:c.878T=
MANE Select
|
NP_001157749.1:p.Leu293=
|
|