ENST00000682275.1:c.957C>T
|
ENSP00000507852.1:p.Ala319=
|
|
ENST00000683395.1:c.898C>T
|
|
|
ENST00000684087.1:c.921C>T
|
ENSP00000506978.1:p.Ala307=
|
|
ENST00000506362.2:c.672C>T
|
ENSP00000424103.2:p.Ala224=
|
|
ENST00000673642.1:c.661-81C>T
|
ENSP00000501242.1:n.661-81C>T
|
|
ENST00000673991.1:c.957C>T
|
ENSP00000501033.1:p.Ala319=
|
|
ENST00000226760.5:c.921C>T
MANE Select
|
ENSP00000226760.1:p.Ala307=
|
|
ENST00000503569.5:c.921C>T
|
ENSP00000423337.1:p.Ala307=
|
|
ENST00000506362.1:c.554C>T
|
|
|
ENST00000507765.1:n.1106C>T
|
|
|
ENST00000513395.1:n.479C>T
|
|
|
NM_001145853.1:c.921C>T
|
NP_001139325.1:p.Ala307=
|
|
NM_006005.3:c.921C>T
MANE Select
|
NP_005996.2:p.Ala307=
|
|
XM_017008586.1:c.930C>T
|
XP_016864075.1:p.Ala310=
|
|