ENST00000554809.6:c.2824C>T
|
ENSP00000450632.2:p.Gln942Ter
|
|
ENST00000555484.2:c.390C>T
|
|
|
ENST00000556250.6:c.4405C>T
|
ENSP00000452033.2:p.Gln1469Ter
|
|
ENST00000557110.2:c.390C>T
|
|
|
ENST00000696642.1:c.*3423C>T
|
ENSP00000512775.1:n.*3423C>T
|
|
ENST00000696644.1:n.348C>T
|
|
|
ENST00000696645.1:n.502C>T
|
|
|
ENST00000696647.1:c.4612C>T
|
ENSP00000512778.1:p.Gln1538Ter
|
|
ENST00000696648.1:c.*2637C>T
|
ENSP00000512779.1:n.*2637C>T
|
|
ENST00000696649.1:c.4456C>T
|
ENSP00000512780.1:p.Gln1486Ter
|
|
ENST00000696650.1:n.4560C>T
|
|
|
ENST00000696659.1:c.2610C>T
|
|
|
ENST00000696663.1:c.3543C>T
|
|
|
ENST00000696664.1:c.3444C>T
|
|
|
ENST00000696665.1:c.390C>T
|
|
|
ENST00000696675.1:c.*368C>T
|
ENSP00000512799.1:n.*368C>T
|
|
ENST00000696683.1:c.3429C>T
|
|
|
ENST00000696684.1:c.3429C>T
|
|
|
ENST00000696685.1:c.3429C>T
|
|
|
ENST00000696686.1:n.1349C>T
|
|
|
ENST00000267430.10:c.4612C>T
MANE Select
|
ENSP00000267430.5:p.Gln1538Ter
|
|
ENST00000267430.9:c.4612C>T
|
ENSP00000267430.5:p.Gln1538Ter
|
|
ENST00000542564.6:c.4534C>T
|
ENSP00000442493.2:p.Gln1512Ter
|
|
ENST00000554809.5:c.1409C>T
|
|
|
ENST00000555013.1:n.445C>T
|
|
|
ENST00000556250.5:c.3160C>T
|
ENSP00000452033.1:p.Gln1054Ter
|
|
NM_001308133.1:c.4534C>T
|
NP_001295062.1:p.Gln1512Ter
|
|
NM_020937.2:c.4612C>T , LRG_502t1:c.4612C>T
|
NP_065988.1:p.Gln1538Ter
|
|
NM_020937.3:c.4612C>T
|
NP_065988.1:p.Gln1538Ter
|
|
XM_011537034.1:c.4627C>T
|
XP_011535336.1:p.Gln1543Ter
|
|
XM_011537035.1:c.4549C>T
|
XP_011535337.1:p.Gln1517Ter
|
|
XM_011537036.1:c.4627C>T
|
XP_011535338.1:p.Gln1543Ter
|
|
XM_011537037.1:c.2641C>T
|
XP_011535339.1:p.Gln881Ter
|
|
XM_011537034.2:c.4627C>T
|
XP_011535336.1:p.Gln1543Ter
|
|
XM_011537035.3:c.4549C>T
|
XP_011535337.1:p.Gln1517Ter
|
|
XM_011537037.3:c.2641C>T
|
XP_011535339.1:p.Gln881Ter
|
|
XM_017021523.1:c.4627C>T
|
XP_016877012.1:p.Gln1543Ter
|
|
XM_017021524.2:c.3664C>T
|
XP_016877013.1:p.Gln1222Ter
|
|
XM_017021525.2:c.3442C>T
|
XP_016877014.1:p.Gln1148Ter
|
|
XM_017021526.2:c.3442C>T
|
XP_016877015.1:p.Gln1148Ter
|
|
XM_017021527.1:c.3427C>T
|
XP_016877016.1:p.Gln1143Ter
|
|
XR_001750470.1:n.4719C>T
|
|
|
XR_001750471.2:n.4704C>T
|
|
|
XR_001750472.1:n.4756C>T
|
|
|
NM_020937.4:c.4612C>T
MANE Select
|
NP_065988.1:p.Gln1538Ter
|
|
NM_001308133.2:c.4534C>T
|
NP_001295062.1:p.Gln1512Ter
|
|