|
ENST00000269217.11:c.4749T>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Thr1583=
|
|
|
ENST00000313654.14:c.9576T>G
MANE Select
|
ENSP00000324532.8:p.Thr3192=
|
|
|
ENST00000649721.1:c.6171T>G
|
ENSP00000497885.1:p.Thr2057=
|
|
|
ENST00000269217.10:c.4749T>G
|
ENSP00000269217.5:p.Thr1583=
|
|
|
ENST00000313654.13:c.9576T>G
|
ENSP00000324532.8:p.Thr3192=
|
|
|
ENST00000399516.7:c.9408T>G
|
ENSP00000382432.2:p.Thr3136=
|
|
|
ENST00000587184.5:c.4581T>G
|
ENSP00000466557.1:p.Thr1527=
|
|
|
ENST00000588004.1:c.97T>G
|
|
|
|
ENST00000588770.5:n.4154T>G
|
|
|
|
NM_000227.4:c.4749T>G
|
NP_000218.3:p.Thr1583=
|
|
|
NM_001127717.2:c.9408T>G
|
NP_001121189.2:p.Thr3136=
|
|
|
NM_001127718.2:c.4581T>G
|
NP_001121190.2:p.Thr1527=
|
|
|
NM_198129.2:c.9576T>G
|
NP_937762.2:p.Thr3192=
|
|
|
XM_011525978.1:c.9603T>G
|
XP_011524280.1:p.Thr3201=
|
|
|
XM_011525979.1:c.9594T>G
|
XP_011524281.1:p.Thr3198=
|
|
|
XM_011525980.1:c.9585T>G
|
XP_011524282.1:p.Thr3195=
|
|
|
XM_011525981.1:c.9471T>G
|
XP_011524283.1:p.Thr3157=
|
|
|
XM_011525982.1:c.9306T>G
|
XP_011524284.1:p.Thr3102=
|
|
|
XM_011525978.2:c.9603T>G
|
XP_011524280.1:p.Thr3201=
|
|
|
XM_011525979.2:c.9594T>G
|
XP_011524281.1:p.Thr3198=
|
|
|
XM_011525980.2:c.9585T>G
|
XP_011524282.1:p.Thr3195=
|
|
|
XM_011525981.2:c.9471T>G
|
XP_011524283.1:p.Thr3157=
|
|
|
XM_011525982.2:c.9306T>G
|
XP_011524284.1:p.Thr3102=
|
|
|
XM_017025743.1:c.7455T>G
|
XP_016881232.1:p.Thr2485=
|
|
|
XM_017025744.1:c.5145T>G
|
XP_016881233.1:p.Thr1715=
|
|
|
XR_001753199.1:n.9844T>G
|
|
|
|
NM_000227.5:c.4749T>G
|
NP_000218.3:p.Thr1583=
|
|
|
NM_001127717.3:c.9408T>G
|
NP_001121189.2:p.Thr3136=
|
|
|
NM_001127718.3:c.4581T>G
|
NP_001121190.2:p.Thr1527=
|
|
|
NM_198129.3:c.9576T>G
|
NP_937762.2:p.Thr3192=
|
|
|
NM_000227.6:c.4749T>G
MANE Plus Clinical
|
NP_000218.3:p.Thr1583=
|
|
|
NM_001127717.4:c.9408T>G
|
NP_001121189.2:p.Thr3136=
|
|
|
NM_001127718.4:c.4581T>G
|
NP_001121190.2:p.Thr1527=
|
|
|
NM_198129.4:c.9576T>G
MANE Select
|
NP_937762.2:p.Thr3192=
|
|
