ENST00000424362.7:c.2933G>A
|
ENSP00000398863.2:p.Gly978Asp
|
|
ENST00000457855.2:c.2915G>A
|
ENSP00000410210.2:p.Gly972Asp
|
|
ENST00000497565.3:n.1555G>A
|
|
|
ENST00000672126.2:c.*550G>A
|
ENSP00000500718.1:n.*550G>A
|
|
ENST00000672515.2:c.2933G>A
|
ENSP00000499951.2:p.Gly978Asp
|
|
ENST00000673551.2:c.*1059G>A
|
ENSP00000500672.1:n.*1059G>A
|
|
ENST00000682208.1:c.2915G>A
|
ENSP00000508123.1:p.Gly972Asp
|
|
ENST00000682980.1:c.2648G>A
|
ENSP00000508198.1:p.Gly883Asp
|
|
ENST00000683423.1:c.*423G>A
|
ENSP00000507659.1:n.*423G>A
|
|
ENST00000683639.1:c.2918G>A
|
ENSP00000506903.1:p.Gly973Asp
|
|
ENST00000683743.1:c.2918G>A
|
ENSP00000507469.1:p.Gly973Asp
|
|
ENST00000684199.1:c.2936G>A
|
ENSP00000506921.1:p.Gly979Asp
|
|
ENST00000684206.1:c.2630G>A
|
ENSP00000507148.1:p.Gly877Asp
|
|
ENST00000684333.1:c.2915G>A
|
ENSP00000508256.1:p.Gly972Asp
|
|
ENST00000684573.1:c.655G>A
|
|
|
ENST00000684608.1:c.*1062G>A
|
ENSP00000507969.1:n.*1062G>A
|
|
ENST00000383829.7:c.2936G>A
MANE Select
|
ENSP00000373340.2:p.Gly979Asp
|
|
ENST00000424362.6:c.2915G>A
|
ENSP00000398863.1:p.Gly972Asp
|
|
ENST00000497565.2:n.1555G>A
|
|
|
ENST00000672126.1:c.2851G>A
|
ENSP00000500718.1:n.2851G>A
|
|
ENST00000672515.1:c.2910G>A
|
|
|
ENST00000673551.1:c.*1059G>A
|
ENSP00000500672.1:n.*1059G>A
|
|
ENST00000383829.6:c.2936G>A
|
ENSP00000373340.2:p.Gly979Asp
|
|
ENST00000424362.5:c.2915G>A
|
ENSP00000398863.1:p.Gly972Asp
|
|
ENST00000433861.6:c.2633G>A
|
ENSP00000402485.2:p.Gly878Asp
|
|
ENST00000457855.1:c.2918G>A
|
ENSP00000410210.1:p.Gly973Asp
|
|
NM_001003694.1:c.2936G>A
|
NP_001003694.1:p.Gly979Asp
|
|
NM_004634.2:c.2918G>A
|
NP_004625.2:p.Gly973Asp
|
|
XM_005265449.1:c.2915G>A
|
XP_005265506.1:p.Gly972Asp
|
|
XM_005265450.1:c.2933G>A
|
XP_005265507.1:p.Gly978Asp
|
|
XM_005265451.1:c.2915G>A
|
XP_005265508.1:p.Gly972Asp
|
|
XM_005265452.1:c.2651G>A
|
XP_005265509.1:p.Gly884Asp
|
|
XM_005265453.1:c.2633G>A
|
XP_005265510.1:p.Gly878Asp
|
|
XM_011534101.1:c.2918G>A
|
XP_011532403.1:p.Gly973Asp
|
|
XM_011534102.1:c.2918G>A
|
XP_011532404.1:p.Gly973Asp
|
|
NM_001319049.1:c.2633G>A
|
NP_001305978.1:p.Gly878Asp
|
|
NM_001319050.1:c.2915G>A
|
NP_001305979.1:p.Gly972Asp
|
|
XM_024453741.1:c.2936G>A
|
XP_024309509.1:p.Gly979Asp
|
|
XM_024453742.1:c.2936G>A
|
XP_024309510.1:p.Gly979Asp
|
|
XM_024453743.1:c.2933G>A
|
XP_024309511.1:p.Gly978Asp
|
|
XM_024453744.1:c.2651G>A
|
XP_024309512.1:p.Gly884Asp
|
|
XR_001740257.1:n.3271G>A
|
|
|
XR_001740258.1:n.3525G>A
|
|
|
NM_001003694.2:c.2936G>A
MANE Select
|
NP_001003694.1:p.Gly979Asp
|
|
NR_160918.1:n.3519G>A
|
|
|
NM_001319049.2:c.2633G>A
|
NP_001305978.1:p.Gly878Asp
|
|
NM_001319050.2:c.2915G>A
|
NP_001305979.1:p.Gly972Asp
|
|
NM_004634.3:c.2918G>A
|
NP_004625.2:p.Gly973Asp
|
|