|
ENST00000371757.7:c.258C>T
MANE Select
|
ENSP00000360822.2:p.Val86=
|
|
|
ENST00000637018.1:n.63C>T
|
|
|
|
ENST00000674572.1:c.99C>T
|
ENSP00000501742.1:p.Val33=
|
|
|
ENST00000675090.1:c.6C>T
|
ENSP00000501833.1:p.Val2=
|
|
|
ENST00000675399.1:c.6C>T
|
ENSP00000501932.1:p.Val2=
|
|
|
ENST00000676421.1:c.6C>T
|
ENSP00000502322.1:p.Val2=
|
|
|
ENST00000263604.5:c.159C>T
|
ENSP00000263604.4:p.Val53=
|
|
|
ENST00000371757.6:c.258C>T
|
ENSP00000360822.2:p.Val86=
|
|
|
ENST00000460750.5:c.258C>T
|
ENSP00000418777.1:p.Val86=
|
|
|
ENST00000473941.5:c.99C>T
|
ENSP00000420764.1:p.Val33=
|
|
|
ENST00000486577.6:c.141C>T
|
ENSP00000417578.3:p.Val47=
|
|
|
ENST00000487664.5:c.258C>T
|
ENSP00000417851.2:p.Val86=
|
|
|
ENST00000488444.6:c.201C>T
|
ENSP00000419007.3:p.Val67=
|
|
|
ENST00000490355.6:c.201C>T
|
ENSP00000418003.3:p.Val67=
|
|
|
ENST00000491806.6:c.201C>T
|
ENSP00000419086.3:p.Val67=
|
|
|
ENST00000628528.2:c.114C>T
|
ENSP00000486374.1:p.Val38=
|
|
|
ENST00000630792.2:c.99C>T
|
ENSP00000486486.1:p.Val33=
|
|
|
ENST00000631073.2:c.201C>T
|
ENSP00000486130.1:p.Val67=
|
|
|
NM_001272003.1:c.114C>T
|
NP_001258932.1:p.Val38=
|
|
|
NM_020822.2:c.258C>T
|
NP_065873.2:p.Val86=
|
|
|
XM_011518877.1:c.393C>T
|
XP_011517179.1:p.Val131=
|
|
|
XM_011518878.1:c.393C>T
|
XP_011517180.1:p.Val131=
|
|
|
XM_011518879.1:c.393C>T
|
XP_011517181.1:p.Val131=
|
|
|
XM_011518880.1:c.159C>T
|
XP_011517182.1:p.Val53=
|
|
|
XM_011518877.3:c.393C>T
|
XP_011517179.1:p.Val131=
|
|
|
XM_011518878.3:c.393C>T
|
XP_011517180.1:p.Val131=
|
|
|
XM_011518879.3:c.393C>T
|
XP_011517181.1:p.Val131=
|
|
|
XM_017014931.1:c.283C>T
|
XP_016870420.1:p.Pro95Ser
|
|
|
XM_017014932.1:c.6C>T
|
XP_016870421.1:p.Val2=
|
|
|
XM_017014933.1:c.-162C>T
|
XP_016870422.1:n.-162C>T
|
|
|
XM_024447617.1:c.-262C>T
|
XP_024303385.1:n.-262C>T
|
|
|
XM_024447618.1:c.-262C>T
|
XP_024303386.1:n.-262C>T
|
|
|
NM_020822.3:c.258C>T
MANE Select
|
NP_065873.2:p.Val86=
|
|
|
NM_001272003.2:c.114C>T
|
NP_001258932.1:p.Val38=
|
|
