|
ENST00000269217.11:c.4145A>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Asp1382Gly
|
|
|
ENST00000313654.14:c.8972A>G
MANE Select
|
ENSP00000324532.8:p.Asp2991Gly
|
|
|
ENST00000649721.1:c.5567A>G
|
ENSP00000497885.1:p.Asp1856Gly
|
|
|
ENST00000269217.10:c.4145A>G
|
ENSP00000269217.5:p.Asp1382Gly
|
|
|
ENST00000313654.13:c.8972A>G
|
ENSP00000324532.8:p.Asp2991Gly
|
|
|
ENST00000399516.7:c.8804A>G
|
ENSP00000382432.2:p.Asp2935Gly
|
|
|
ENST00000587184.5:c.3977A>G
|
ENSP00000466557.1:p.Asp1326Gly
|
|
|
ENST00000588770.5:n.3550A>G
|
|
|
|
NM_000227.4:c.4145A>G
|
NP_000218.3:p.Asp1382Gly
|
|
|
NM_001127717.2:c.8804A>G
|
NP_001121189.2:p.Asp2935Gly
|
|
|
NM_001127718.2:c.3977A>G
|
NP_001121190.2:p.Asp1326Gly
|
|
|
NM_198129.2:c.8972A>G
|
NP_937762.2:p.Asp2991Gly
|
|
|
XM_011525978.1:c.8999A>G
|
XP_011524280.1:p.Asp3000Gly
|
|
|
XM_011525979.1:c.8990A>G
|
XP_011524281.1:p.Asp2997Gly
|
|
|
XM_011525980.1:c.8981A>G
|
XP_011524282.1:p.Asp2994Gly
|
|
|
XM_011525981.1:c.8867A>G
|
XP_011524283.1:p.Asp2956Gly
|
|
|
XM_011525982.1:c.8702A>G
|
XP_011524284.1:p.Asp2901Gly
|
|
|
XM_011525978.2:c.8999A>G
|
XP_011524280.1:p.Asp3000Gly
|
|
|
XM_011525979.2:c.8990A>G
|
XP_011524281.1:p.Asp2997Gly
|
|
|
XM_011525980.2:c.8981A>G
|
XP_011524282.1:p.Asp2994Gly
|
|
|
XM_011525981.2:c.8867A>G
|
XP_011524283.1:p.Asp2956Gly
|
|
|
XM_011525982.2:c.8702A>G
|
XP_011524284.1:p.Asp2901Gly
|
|
|
XM_017025743.1:c.6851A>G
|
XP_016881232.1:p.Asp2284Gly
|
|
|
XM_017025744.1:c.4541A>G
|
XP_016881233.1:p.Asp1514Gly
|
|
|
XR_001753199.1:n.9240A>G
|
|
|
|
NM_000227.5:c.4145A>G
|
NP_000218.3:p.Asp1382Gly
|
|
|
NM_001127717.3:c.8804A>G
|
NP_001121189.2:p.Asp2935Gly
|
|
|
NM_001127718.3:c.3977A>G
|
NP_001121190.2:p.Asp1326Gly
|
|
|
NM_198129.3:c.8972A>G
|
NP_937762.2:p.Asp2991Gly
|
|
|
NM_000227.6:c.4145A>G
MANE Plus Clinical
|
NP_000218.3:p.Asp1382Gly
|
|
|
NM_001127717.4:c.8804A>G
|
NP_001121189.2:p.Asp2935Gly
|
|
|
NM_001127718.4:c.3977A>G
|
NP_001121190.2:p.Asp1326Gly
|
|
|
NM_198129.4:c.8972A>G
MANE Select
|
NP_937762.2:p.Asp2991Gly
|
|
