ENST00000313863.11:c.*4C>G
|
ENSP00000316631.6:n.*4C>G
|
|
ENST00000393119.7:c.1592C>G
MANE Select
|
ENSP00000376827.2:p.Ala531Gly
|
|
ENST00000537529.7:c.1163C>G
|
ENSP00000442096.3:p.Ala388Gly
|
|
ENST00000675753.2:c.*1211C>G
|
ENSP00000502156.1:n.*1211C>G
|
|
ENST00000676787.1:c.1463C>G
|
ENSP00000503999.1:p.Ala488Gly
|
|
ENST00000677111.1:c.*1066C>G
|
ENSP00000504282.1:n.*1066C>G
|
|
ENST00000677160.1:n.2866C>G
|
|
|
ENST00000677416.1:n.2913C>G
|
|
|
ENST00000677486.1:c.*936C>G
|
ENSP00000503852.1:n.*936C>G
|
|
ENST00000677709.1:n.2292C>G
|
|
|
ENST00000678011.1:n.2492C>G
|
|
|
ENST00000678432.1:c.*1366C>G
|
ENSP00000504452.1:n.*1366C>G
|
|
ENST00000678463.1:c.1509C>G
|
ENSP00000502984.1:p.Gly503=
|
|
ENST00000678568.1:c.*916C>G
|
ENSP00000504754.1:n.*916C>G
|
|
ENST00000678641.1:c.*936C>G
|
ENSP00000503159.1:n.*936C>G
|
|
ENST00000678763.1:n.1907C>G
|
|
|
ENST00000313863.10:c.*4C>G
|
ENSP00000316631.6:n.*4C>G
|
|
ENST00000393119.6:c.1592C>G
|
ENSP00000376827.2:p.Ala531Gly
|
|
ENST00000393120.6:c.*999C>G
|
ENSP00000376828.2:n.*999C>G
|
|
ENST00000537529.6:c.1562C>G
|
ENSP00000442096.2:p.Ala521Gly
|
|
ENST00000583577.1:n.418C>G
|
|
|
NM_001165927.1:c.1562C>G , LRG_687t2:c.1562C>G
|
NP_001159399.1:p.Ala521Gly
|
|
NM_017777.3:c.1592C>G , LRG_687t1:c.1592C>G
|
NP_060247.2:p.Ala531Gly
|
|
XM_005257483.3:c.1509C>G
|
XP_005257540.1:p.Gly503=
|
|
XM_005257485.3:c.1080C>G
|
XP_005257542.1:p.Gly360=
|
|
XM_005257486.3:c.983C>G
|
XP_005257543.1:p.Ala328Gly
|
|
XM_006721965.2:c.900C>G
|
XP_006722028.1:p.Gly300=
|
|
XM_011524957.1:c.1518C>G
|
XP_011523259.1:p.Gly506=
|
|
XM_011524958.1:c.1601C>G
|
XP_011523260.1:p.Ala534Gly
|
|
XM_011524959.1:c.*4C>G
|
XP_011523261.1:n.*4C>G
|
|
NM_001321268.1:c.983C>G
|
NP_001308197.1:p.Ala328Gly
|
|
NM_001321269.1:c.1509C>G
|
NP_001308198.1:p.Gly503=
|
|
NM_001330397.1:c.*4C>G
|
NP_001317326.1:n.*4C>G
|
|
XM_005257485.4:c.1080C>G
|
XP_005257542.1:p.Gly360=
|
|
XM_006721965.3:c.900C>G
|
XP_006722028.1:p.Gly300=
|
|
XM_011524957.2:c.1518C>G
|
XP_011523259.1:p.Gly506=
|
|
XM_011524958.2:c.1601C>G
|
XP_011523260.1:p.Ala534Gly
|
|
XM_011524959.2:c.*4C>G
|
XP_011523261.1:n.*4C>G
|
|
XM_017024805.1:c.1163C>G
|
XP_016880294.1:p.Ala388Gly
|
|
XR_002958042.1:n.1520C>G
|
|
|
NM_001321268.2:c.983C>G
|
NP_001308197.1:p.Ala328Gly
|
|
NM_001321269.2:c.1509C>G
|
NP_001308198.1:p.Gly503=
|
|
NM_001330397.2:c.*4C>G
|
NP_001317326.1:n.*4C>G
|
|
NM_017777.4:c.1592C>G
MANE Select
|
NP_060247.2:p.Ala531Gly
|
|