|
NM_020937.4:c.5745A>G
MANE Select
|
NP_065988.1:p.Thr1915=
|
|
ENST00000267430.10:c.5745A>G
MANE Select
|
ENSP00000267430.5:p.Thr1915=
|
|
NM_001308133.1:c.5667A>G
|
NP_001295062.1:p.Thr1889=
|
|
NM_001308133.2:c.5667A>G
|
NP_001295062.1:p.Thr1889=
|
|
NM_020937.2:c.5745A>G , LRG_502t1:c.5745A>G
|
NP_065988.1:p.Thr1915=
|
|
NM_020937.3:c.5745A>G
|
NP_065988.1:p.Thr1915=
|
|
ENST00000267430.9:c.5745A>G
|
ENSP00000267430.5:p.Thr1915=
|
|
ENST00000542564.6:c.5667A>G
|
ENSP00000442493.2:p.Thr1889=
|
|
ENST00000553551.1:n.238A>G
|
|
|
ENST00000553551.2:n.1945A>G
|
|
|
ENST00000554809.5:c.2647A>G
|
|
|
ENST00000554809.6:c.4062A>G
|
ENSP00000450632.2:p.Thr1354=
|
|
ENST00000555484.1:c.123A>G
|
ENSP00000450797.1:p.Thr41=
|
|
ENST00000555484.2:c.1523A>G
|
|
|
ENST00000556250.5:c.4293A>G
|
ENSP00000452033.1:p.Thr1431=
|
|
ENST00000556250.6:c.5538A>G
|
ENSP00000452033.2:p.Thr1846=
|
|
ENST00000557110.1:c.377-60A>G
|
ENSP00000451846.1:n.377-60A>G
|
|
ENST00000557110.2:c.1495-60A>G
|
|
|
ENST00000696645.1:n.1635A>G
|
|
|
ENST00000696647.1:c.5369A>G
|
ENSP00000512778.1:p.Gln1790Arg
|
|
ENST00000696648.1:c.*3770A>G
|
ENSP00000512779.1:n.*3770A>G
|
|
ENST00000696649.1:c.5589A>G
|
ENSP00000512780.1:p.Thr1863=
|
|
ENST00000696651.1:n.2185A>G
|
|
|
ENST00000696659.1:c.3367A>G
|
|
|
ENST00000696663.1:c.4676A>G
|
|
|
ENST00000696664.1:c.4577A>G
|
|
|
ENST00000696665.1:c.1495-1198A>G
|
|
|
ENST00000696675.1:c.*1501A>G
|
ENSP00000512799.1:n.*1501A>G
|
|
ENST00000696683.1:c.4373A>G
|
|
|
ENST00000696684.1:c.4158-1198A>G
|
|
|
ENST00000696685.1:c.4563A>G
|
|
|
ENST00000696686.1:n.2482A>G
|
|
|
XM_011537034.1:c.5760A>G
|
XP_011535336.1:p.Thr1920=
|
|
XM_011537034.2:c.5760A>G
|
XP_011535336.1:p.Thr1920=
|
|
XM_011537035.1:c.5682A>G
|
XP_011535337.1:p.Thr1894=
|
|
XM_011537035.3:c.5682A>G
|
XP_011535337.1:p.Thr1894=
|
|
XM_011537036.1:c.5384A>G
|
XP_011535338.1:p.Gln1795Arg
|
|
XM_011537037.1:c.3774A>G
|
XP_011535339.1:p.Thr1258=
|
|
XM_011537037.3:c.3774A>G
|
XP_011535339.1:p.Thr1258=
|
|
XM_017021523.1:c.5356-1198A>G
|
XP_016877012.1:n.5356-1198A>G
|
|
XM_017021524.2:c.4797A>G
|
XP_016877013.1:p.Thr1599=
|
|
XM_017021525.2:c.4575A>G
|
XP_016877014.1:p.Thr1525=
|
|
XM_017021526.2:c.4575A>G
|
XP_016877015.1:p.Thr1525=
|
|
XM_017021527.1:c.4560A>G
|
XP_016877016.1:p.Thr1520=
|
|
XR_001750470.1:n.5476A>G
|
|
|
XR_001750471.2:n.5461A>G
|
|
