|
ENST00000269217.11:c.1431T>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Thr477=
|
|
|
ENST00000313654.14:c.6258T>G
MANE Select
|
ENSP00000324532.8:p.Thr2086=
|
|
|
ENST00000649721.1:c.3150T>G
|
ENSP00000497885.1:p.Thr1050=
|
|
|
ENST00000269217.10:c.1431T>G
|
ENSP00000269217.5:p.Thr477=
|
|
|
ENST00000313654.13:c.6258T>G
|
ENSP00000324532.8:p.Thr2086=
|
|
|
ENST00000399516.7:c.6090T>G
|
ENSP00000382432.2:p.Thr2030=
|
|
|
ENST00000586751.5:c.1036T>G
|
|
|
|
ENST00000587184.5:c.1263T>G
|
ENSP00000466557.1:p.Thr421=
|
|
|
ENST00000588770.5:n.836T>G
|
|
|
|
NM_000227.4:c.1431T>G
|
NP_000218.3:p.Thr477=
|
|
|
NM_001127717.2:c.6090T>G
|
NP_001121189.2:p.Thr2030=
|
|
|
NM_001127718.2:c.1263T>G
|
NP_001121190.2:p.Thr421=
|
|
|
NM_198129.2:c.6258T>G
|
NP_937762.2:p.Thr2086=
|
|
|
XM_011525978.1:c.6285T>G
|
XP_011524280.1:p.Thr2095=
|
|
|
XM_011525979.1:c.6276T>G
|
XP_011524281.1:p.Thr2092=
|
|
|
XM_011525980.1:c.6267T>G
|
XP_011524282.1:p.Thr2089=
|
|
|
XM_011525981.1:c.6153T>G
|
XP_011524283.1:p.Thr2051=
|
|
|
XM_011525982.1:c.6285T>G
|
XP_011524284.1:p.Thr2095=
|
|
|
XM_011525978.2:c.6285T>G
|
XP_011524280.1:p.Thr2095=
|
|
|
XM_011525979.2:c.6276T>G
|
XP_011524281.1:p.Thr2092=
|
|
|
XM_011525980.2:c.6267T>G
|
XP_011524282.1:p.Thr2089=
|
|
|
XM_011525981.2:c.6153T>G
|
XP_011524283.1:p.Thr2051=
|
|
|
XM_011525982.2:c.6285T>G
|
XP_011524284.1:p.Thr2095=
|
|
|
XM_017025743.1:c.4137T>G
|
XP_016881232.1:p.Thr1379=
|
|
|
XM_017025744.1:c.1827T>G
|
XP_016881233.1:p.Thr609=
|
|
|
XR_001753199.1:n.6526T>G
|
|
|
|
NM_000227.5:c.1431T>G
|
NP_000218.3:p.Thr477=
|
|
|
NM_001127717.3:c.6090T>G
|
NP_001121189.2:p.Thr2030=
|
|
|
NM_001127718.3:c.1263T>G
|
NP_001121190.2:p.Thr421=
|
|
|
NM_198129.3:c.6258T>G
|
NP_937762.2:p.Thr2086=
|
|
|
NM_000227.6:c.1431T>G
MANE Plus Clinical
|
NP_000218.3:p.Thr477=
|
|
|
NM_001127717.4:c.6090T>G
|
NP_001121189.2:p.Thr2030=
|
|
|
NM_001127718.4:c.1263T>G
|
NP_001121190.2:p.Thr421=
|
|
|
NM_198129.4:c.6258T>G
MANE Select
|
NP_937762.2:p.Thr2086=
|
|
