ENST00000529510.6:n.1014+309A=
|
|
|
ENST00000697845.1:n.1247A=
|
|
|
ENST00000697846.1:n.1014+309A=
|
|
|
ENST00000697847.1:n.1075A=
|
|
|
ENST00000697848.1:n.1075A=
|
|
|
ENST00000697849.1:n.2362A=
|
|
|
ENST00000697850.1:n.1075A=
|
|
|
ENST00000697851.1:n.2683A=
|
|
|
ENST00000638186.1:n.1149A=
|
|
|
ENST00000638360.1:n.981A=
|
|
|
ENST00000638925.1:n.1082A=
|
|
|
ENST00000650539.1:n.1251A=
|
|
|
ENST00000330775.9:c.845A=
|
ENSP00000476242.2:p.Tyr282=
|
|
ENST00000357590.9:c.845A=
|
ENSP00000476176.2:p.Tyr282=
|
|
ENST00000524428.5:n.1106+309A=
|
|
|
ENST00000525039.5:n.1269A=
|
|
|
ENST00000525102.5:n.1603A=
|
|
|
ENST00000525372.5:n.846A=
|
|
|
ENST00000526275.5:n.1627A=
|
|
|
ENST00000527992.5:n.1073A=
|
|
|
ENST00000529510.5:n.558+309A=
|
|
|
ENST00000530407.5:n.995A=
|
|
|
ENST00000532085.1:n.3704A=
|
|
|
ENST00000538950.5:c.626A=
|
ENSP00000475991.2:p.Tyr209=
|
|
ENST00000545985.5:c.845A=
|
ENSP00000475241.2:p.Tyr282=
|
|
NM_001164277.1:c.845A= , LRG_187t1:c.845A=
|
NP_001157749.1:p.Tyr282=
|
|
NM_001164278.1:c.845A=
|
NP_001157750.1:p.Tyr282=
|
|
NM_001164279.1:c.626A=
|
NP_001157751.1:p.Tyr209=
|
|
NM_001164280.1:c.845A=
|
NP_001157752.1:p.Tyr282=
|
|
NM_001467.5:c.845A=
|
NP_001458.1:p.Tyr282=
|
|
NM_001164278.2:c.845A=
|
NP_001157750.1:p.Tyr282=
|
|
NM_001164279.2:c.626A=
|
NP_001157751.1:p.Tyr209=
|
|
NM_001164280.2:c.845A=
|
NP_001157752.1:p.Tyr282=
|
|
NM_001467.6:c.845A=
|
NP_001458.1:p.Tyr282=
|
|
NM_001164277.2:c.845A=
MANE Select
|
NP_001157749.1:p.Tyr282=
|
|