ENST00000682275.1:c.1073C>G
|
ENSP00000507852.1:p.Pro358Arg
|
|
ENST00000683395.1:c.1014C>G
|
|
|
ENST00000684087.1:c.1037C>G
|
ENSP00000506978.1:p.Pro346Arg
|
|
ENST00000506362.2:c.788C>G
|
ENSP00000424103.2:p.Pro263Arg
|
|
ENST00000673642.1:c.696C>G
|
ENSP00000501242.1:p.Pro232=
|
|
ENST00000673991.1:c.1073C>G
|
ENSP00000501033.1:p.Pro358Arg
|
|
ENST00000226760.5:c.1037C>G
MANE Select
|
ENSP00000226760.1:p.Pro346Arg
|
|
ENST00000503569.5:c.1037C>G
|
ENSP00000423337.1:p.Pro346Arg
|
|
ENST00000506362.1:c.670C>G
|
|
|
ENST00000507765.1:n.1222C>G
|
|
|
NM_001145853.1:c.1037C>G
|
NP_001139325.1:p.Pro346Arg
|
|
NM_006005.3:c.1037C>G
MANE Select
|
NP_005996.2:p.Pro346Arg
|
|
XM_017008586.1:c.1046C>G
|
XP_016864075.1:p.Pro349Arg
|
|