ENST00000554809.6:c.2829T=
|
ENSP00000450632.2:p.Asp943=
|
|
ENST00000555484.2:c.395T=
|
|
|
ENST00000556250.6:c.4410T=
|
ENSP00000452033.2:p.Asp1470=
|
|
ENST00000557110.2:c.395T=
|
|
|
ENST00000696642.1:c.*3428T=
|
ENSP00000512775.1:n.*3428T=
|
|
ENST00000696644.1:n.353T=
|
|
|
ENST00000696645.1:n.507T=
|
|
|
ENST00000696647.1:c.4617T=
|
ENSP00000512778.1:p.Asp1539=
|
|
ENST00000696648.1:c.*2642T=
|
ENSP00000512779.1:n.*2642T=
|
|
ENST00000696649.1:c.4461T=
|
ENSP00000512780.1:p.Asp1487=
|
|
ENST00000696650.1:n.4565T=
|
|
|
ENST00000696659.1:c.2615T=
|
|
|
ENST00000696663.1:c.3548T=
|
|
|
ENST00000696664.1:c.3449T=
|
|
|
ENST00000696665.1:c.395T=
|
|
|
ENST00000696675.1:c.*373T=
|
ENSP00000512799.1:n.*373T=
|
|
ENST00000696683.1:c.3434T=
|
|
|
ENST00000696684.1:c.3434T=
|
|
|
ENST00000696685.1:c.3434T=
|
|
|
ENST00000696686.1:n.1354T=
|
|
|
ENST00000267430.10:c.4617T=
MANE Select
|
ENSP00000267430.5:p.Asp1539=
|
|
ENST00000267430.9:c.4617T=
|
ENSP00000267430.5:p.Asp1539=
|
|
ENST00000542564.6:c.4539T=
|
ENSP00000442493.2:p.Asp1513=
|
|
ENST00000554809.5:c.1414T=
|
|
|
ENST00000555013.1:n.450T=
|
|
|
ENST00000556250.5:c.3165T=
|
ENSP00000452033.1:p.Asp1055=
|
|
NM_001308133.1:c.4539T=
|
NP_001295062.1:p.Asp1513=
|
|
NM_020937.2:c.4617T= , LRG_502t1:c.4617T=
|
NP_065988.1:p.Asp1539=
|
|
NM_020937.3:c.4617T=
|
NP_065988.1:p.Asp1539=
|
|
XM_011537034.1:c.4632T=
|
XP_011535336.1:p.Asp1544=
|
|
XM_011537035.1:c.4554T=
|
XP_011535337.1:p.Asp1518=
|
|
XM_011537036.1:c.4632T=
|
XP_011535338.1:p.Asp1544=
|
|
XM_011537037.1:c.2646T=
|
XP_011535339.1:p.Asp882=
|
|
XM_011537034.2:c.4632T=
|
XP_011535336.1:p.Asp1544=
|
|
XM_011537035.3:c.4554T=
|
XP_011535337.1:p.Asp1518=
|
|
XM_011537037.3:c.2646T=
|
XP_011535339.1:p.Asp882=
|
|
XM_017021523.1:c.4632T=
|
XP_016877012.1:p.Asp1544=
|
|
XM_017021524.2:c.3669T=
|
XP_016877013.1:p.Asp1223=
|
|
XM_017021525.2:c.3447T=
|
XP_016877014.1:p.Asp1149=
|
|
XM_017021526.2:c.3447T=
|
XP_016877015.1:p.Asp1149=
|
|
XM_017021527.1:c.3432T=
|
XP_016877016.1:p.Asp1144=
|
|
XR_001750470.1:n.4724T=
|
|
|
XR_001750471.2:n.4709T=
|
|
|
XR_001750472.1:n.4761T=
|
|
|
NM_020937.4:c.4617T=
MANE Select
|
NP_065988.1:p.Asp1539=
|
|
NM_001308133.2:c.4539T=
|
NP_001295062.1:p.Asp1513=
|
|