|
ENST00000269217.11:c.3432T>G
MANE Plus Clinical
|
ENSP00000269217.5:p.Thr1144=
|
|
|
ENST00000313654.14:c.8259T>G
MANE Select
|
ENSP00000324532.8:p.Thr2753=
|
|
|
ENST00000649721.1:c.4854T>G
|
ENSP00000497885.1:p.Thr1618=
|
|
|
ENST00000269217.10:c.3432T>G
|
ENSP00000269217.5:p.Thr1144=
|
|
|
ENST00000313654.13:c.8259T>G
|
ENSP00000324532.8:p.Thr2753=
|
|
|
ENST00000399516.7:c.8091T>G
|
ENSP00000382432.2:p.Thr2697=
|
|
|
ENST00000586751.5:c.3037T>G
|
|
|
|
ENST00000587184.5:c.3264T>G
|
ENSP00000466557.1:p.Thr1088=
|
|
|
ENST00000588770.5:n.2837T>G
|
|
|
|
NM_000227.4:c.3432T>G
|
NP_000218.3:p.Thr1144=
|
|
|
NM_001127717.2:c.8091T>G
|
NP_001121189.2:p.Thr2697=
|
|
|
NM_001127718.2:c.3264T>G
|
NP_001121190.2:p.Thr1088=
|
|
|
NM_198129.2:c.8259T>G
|
NP_937762.2:p.Thr2753=
|
|
|
XM_011525978.1:c.8286T>G
|
XP_011524280.1:p.Thr2762=
|
|
|
XM_011525979.1:c.8277T>G
|
XP_011524281.1:p.Thr2759=
|
|
|
XM_011525980.1:c.8268T>G
|
XP_011524282.1:p.Thr2756=
|
|
|
XM_011525981.1:c.8154T>G
|
XP_011524283.1:p.Thr2718=
|
|
|
XM_011525982.1:c.7989T>G
|
XP_011524284.1:p.Thr2663=
|
|
|
XM_011525978.2:c.8286T>G
|
XP_011524280.1:p.Thr2762=
|
|
|
XM_011525979.2:c.8277T>G
|
XP_011524281.1:p.Thr2759=
|
|
|
XM_011525980.2:c.8268T>G
|
XP_011524282.1:p.Thr2756=
|
|
|
XM_011525981.2:c.8154T>G
|
XP_011524283.1:p.Thr2718=
|
|
|
XM_011525982.2:c.7989T>G
|
XP_011524284.1:p.Thr2663=
|
|
|
XM_017025743.1:c.6138T>G
|
XP_016881232.1:p.Thr2046=
|
|
|
XM_017025744.1:c.3828T>G
|
XP_016881233.1:p.Thr1276=
|
|
|
XR_001753199.1:n.8527T>G
|
|
|
|
NM_000227.5:c.3432T>G
|
NP_000218.3:p.Thr1144=
|
|
|
NM_001127717.3:c.8091T>G
|
NP_001121189.2:p.Thr2697=
|
|
|
NM_001127718.3:c.3264T>G
|
NP_001121190.2:p.Thr1088=
|
|
|
NM_198129.3:c.8259T>G
|
NP_937762.2:p.Thr2753=
|
|
|
NM_000227.6:c.3432T>G
MANE Plus Clinical
|
NP_000218.3:p.Thr1144=
|
|
|
NM_001127717.4:c.8091T>G
|
NP_001121189.2:p.Thr2697=
|
|
|
NM_001127718.4:c.3264T>G
|
NP_001121190.2:p.Thr1088=
|
|
|
NM_198129.4:c.8259T>G
MANE Select
|
NP_937762.2:p.Thr2753=
|
|
