|
ENST00000395762.7:c.1574A>G
MANE Select
|
ENSP00000379111.2:p.Glu525Gly
|
|
|
ENST00000170630.6:c.1529A>G
|
ENSP00000170630.3:p.Glu510Gly
|
|
|
ENST00000395762.6:c.1574A>G
|
ENSP00000379111.2:p.Glu525Gly
|
|
|
ENST00000543915.6:c.1574A>G
|
ENSP00000441667.2:p.Glu525Gly
|
|
|
ENST00000565352.1:c.230-1177A>G
|
ENSP00000461268.1:n.230-1177A>G
|
|
|
ENST00000568746.5:c.*1617A>G
|
ENSP00000455714.1:n.*1617A>G
|
|
|
NM_000418.3:c.1574A>G
|
NP_000409.1:p.Glu525Gly
|
|
|
NM_001257406.1:c.1574A>G
|
NP_001244335.1:p.Glu525Gly
|
|
|
NM_001257407.1:c.1529A>G
|
NP_001244336.1:p.Glu510Gly
|
|
|
NM_001257997.1:c.1094A>G
|
NP_001244926.1:p.Glu365Gly
|
|
|
XM_005255308.2:c.683A>G
|
XP_005255365.1:p.Glu228Gly
|
|
|
XM_006721043.1:c.623A>G
|
XP_006721106.1:p.Glu208Gly
|
|
|
XM_011545825.1:c.1574A>G
|
XP_011544127.1:p.Glu525Gly
|
|
|
XM_011545826.1:c.1574A>G
|
XP_011544128.1:p.Glu525Gly
|
|
|
XM_011545827.1:c.1574A>G
|
XP_011544129.1:p.Glu525Gly
|
|
|
XM_011545828.1:c.1307A>G
|
XP_011544130.1:p.Glu436Gly
|
|
|
XM_011545829.1:c.1277A>G
|
XP_011544131.1:p.Glu426Gly
|
|
|
XM_011545830.1:c.1277A>G
|
XP_011544132.1:p.Glu426Gly
|
|
|
XM_011545831.1:c.1277A>G
|
XP_011544133.1:p.Glu426Gly
|
|
|
XM_011545832.1:c.1277A>G
|
XP_011544134.1:p.Glu426Gly
|
|
|
XM_011545833.1:c.1277A>G
|
XP_011544135.1:p.Glu426Gly
|
|
|
XM_011545834.1:c.1151A>G
|
XP_011544136.1:p.Glu384Gly
|
|
|
XM_011545826.2:c.1574A>G
|
XP_011544128.1:p.Glu525Gly
|
|
|
XM_011545827.2:c.1574A>G
|
XP_011544129.1:p.Glu525Gly
|
|
|
XM_011545828.2:c.1307A>G
|
XP_011544130.1:p.Glu436Gly
|
|
|
XM_011545830.2:c.1277A>G
|
XP_011544132.1:p.Glu426Gly
|
|
|
XM_011545833.2:c.1277A>G
|
XP_011544135.1:p.Glu426Gly
|
|
|
XM_011545834.2:c.1151A>G
|
XP_011544136.1:p.Glu384Gly
|
|
|
NM_000418.4:c.1574A>G
MANE Select
|
NP_000409.1:p.Glu525Gly
|
|
|
NM_001257406.2:c.1574A>G
|
NP_001244335.1:p.Glu525Gly
|
|
|
NM_001257407.2:c.1529A>G
|
NP_001244336.1:p.Glu510Gly
|
|
|
NM_001257997.2:c.1094A>G
|
NP_001244926.1:p.Glu365Gly
|
|
