ENST00000682275.1:c.2328_2329delinsCT
|
ENSP00000507852.1:p.Pro776=
|
|
ENST00000683395.1:c.2269_2270delinsCT
|
|
|
ENST00000684087.1:c.2292_2293delinsCT
|
ENSP00000506978.1:p.Pro764=
|
|
ENST00000506362.2:c.2043_2044delinsCT
|
ENSP00000424103.2:p.Pro681=
|
|
ENST00000673642.1:c.1951_1952delinsCT
|
ENSP00000501242.1:n.1951_1952delinsCT
|
|
ENST00000673991.1:c.2328_2329delinsCT
|
ENSP00000501033.1:p.Pro776=
|
|
ENST00000226760.5:c.2292_2293delinsCT
MANE Select
|
ENSP00000226760.1:p.Pro764=
|
|
ENST00000503569.5:c.2292_2293delinsCT
|
ENSP00000423337.1:p.Pro764=
|
|
ENST00000507765.1:n.2477_2478delinsCT
|
|
|
NM_001145853.1:c.2292_2293delinsCT
|
NP_001139325.1:p.Pro764=
|
|
NM_006005.3:c.2292_2293delinsCT
MANE Select
|
NP_005996.2:p.Pro764=
|
|
XM_017008586.1:c.2301_2302delinsCT
|
XP_016864075.1:p.Pro767=
|
|