ENST00000313863.11:c.*20G>T
|
ENSP00000316631.6:n.*20G>T
|
|
ENST00000393119.7:c.1608G>T
MANE Select
|
ENSP00000376827.2:p.Arg536=
|
|
ENST00000537529.7:c.1179G>T
|
ENSP00000442096.3:p.Arg393=
|
|
ENST00000675753.2:c.*1227G>T
|
ENSP00000502156.1:n.*1227G>T
|
|
ENST00000676787.1:c.1479G>T
|
ENSP00000503999.1:p.Arg493=
|
|
ENST00000677111.1:c.*1082G>T
|
ENSP00000504282.1:n.*1082G>T
|
|
ENST00000677160.1:n.2882G>T
|
|
|
ENST00000677416.1:n.2929G>T
|
|
|
ENST00000677486.1:c.*952G>T
|
ENSP00000503852.1:n.*952G>T
|
|
ENST00000677709.1:n.2308G>T
|
|
|
ENST00000678011.1:n.2508G>T
|
|
|
ENST00000678432.1:c.*1382G>T
|
ENSP00000504452.1:n.*1382G>T
|
|
ENST00000678463.1:c.1525G>T
|
ENSP00000502984.1:p.Ala509Ser
|
|
ENST00000678568.1:c.*932G>T
|
ENSP00000504754.1:n.*932G>T
|
|
ENST00000678641.1:c.*952G>T
|
ENSP00000503159.1:n.*952G>T
|
|
ENST00000678763.1:n.1923G>T
|
|
|
ENST00000313863.10:c.*20G>T
|
ENSP00000316631.6:n.*20G>T
|
|
ENST00000393119.6:c.1608G>T
|
ENSP00000376827.2:p.Arg536=
|
|
ENST00000393120.6:c.*1015G>T
|
ENSP00000376828.2:n.*1015G>T
|
|
ENST00000537529.6:c.1578G>T
|
ENSP00000442096.2:p.Arg526=
|
|
ENST00000583577.1:n.434G>T
|
|
|
NM_001165927.1:c.1578G>T , LRG_687t2:c.1578G>T
|
NP_001159399.1:p.Arg526=
|
|
NM_017777.3:c.1608G>T , LRG_687t1:c.1608G>T
|
NP_060247.2:p.Arg536=
|
|
XM_005257483.3:c.1525G>T
|
XP_005257540.1:p.Ala509Ser
|
|
XM_005257485.3:c.1096G>T
|
XP_005257542.1:p.Ala366Ser
|
|
XM_005257486.3:c.999G>T
|
XP_005257543.1:p.Arg333=
|
|
XM_006721965.2:c.916G>T
|
XP_006722028.1:p.Ala306Ser
|
|
XM_011524957.1:c.1534G>T
|
XP_011523259.1:p.Ala512Ser
|
|
XM_011524958.1:c.1617G>T
|
XP_011523260.1:p.Arg539=
|
|
XM_011524959.1:c.*20G>T
|
XP_011523261.1:n.*20G>T
|
|
NM_001321268.1:c.999G>T
|
NP_001308197.1:p.Arg333=
|
|
NM_001321269.1:c.1525G>T
|
NP_001308198.1:p.Ala509Ser
|
|
NM_001330397.1:c.*20G>T
|
NP_001317326.1:n.*20G>T
|
|
XM_005257485.4:c.1096G>T
|
XP_005257542.1:p.Ala366Ser
|
|
XM_006721965.3:c.916G>T
|
XP_006722028.1:p.Ala306Ser
|
|
XM_011524957.2:c.1534G>T
|
XP_011523259.1:p.Ala512Ser
|
|
XM_011524958.2:c.1617G>T
|
XP_011523260.1:p.Arg539=
|
|
XM_011524959.2:c.*20G>T
|
XP_011523261.1:n.*20G>T
|
|
XM_017024805.1:c.1179G>T
|
XP_016880294.1:p.Arg393=
|
|
XR_002958042.1:n.1536G>T
|
|
|
NM_001321268.2:c.999G>T
|
NP_001308197.1:p.Arg333=
|
|
NM_001321269.2:c.1525G>T
|
NP_001308198.1:p.Ala509Ser
|
|
NM_001330397.2:c.*20G>T
|
NP_001317326.1:n.*20G>T
|
|
NM_017777.4:c.1608G>T
MANE Select
|
NP_060247.2:p.Arg536=
|
|