ENST00000342245.9:c.1489T>G
MANE Select
|
ENSP00000340409.4:p.Tyr497Asp
|
|
ENST00000342245.8:c.1489T>G
|
ENSP00000340409.4:p.Tyr497Asp
|
|
ENST00000526280.1:c.546T>G
|
|
|
ENST00000527275.5:c.1486T>G
|
ENSP00000435350.1:p.Tyr496Asp
|
|
ENST00000531303.5:c.*340T>G
|
ENSP00000432625.1:n.*340T>G
|
|
ENST00000531336.1:n.477T>G
|
|
|
ENST00000533123.5:c.*216T>G
|
ENSP00000435950.1:n.*216T>G
|
|
ENST00000534405.5:c.*320T>G
|
ENSP00000434353.1:n.*320T>G
|
|
NM_000543.4:c.1489T>G
|
NP_000534.3:p.Tyr497Asp
|
|
NM_001007593.2:c.1486T>G
|
NP_001007594.2:p.Tyr496Asp
|
|
XM_005253075.3:c.1509T>G
|
XP_005253132.1:p.Val503=
|
|
XM_011520303.1:c.1357T>G
|
XP_011518605.1:p.Tyr453Asp
|
|
XM_011520304.1:c.1377T>G
|
XP_011518606.1:p.Val459=
|
|
NM_001318087.1:c.1509T>G
|
NP_001305016.1:p.Val503=
|
|
NM_001318088.1:c.568T>G
|
NP_001305017.1:p.Tyr190Asp
|
|
NM_001365135.1:c.1357T>G
|
NP_001352064.1:p.Tyr453Asp
|
|
NR_027400.2:n.1502T>G
|
|
|
NR_134502.1:n.1041T>G
|
|
|
XM_011520304.2:c.1377T>G
|
XP_011518606.1:p.Val459=
|
|
XR_001747940.2:n.1674T>G
|
|
|
XR_002957158.1:n.1856T>G
|
|
|
NM_000543.5:c.1489T>G
MANE Select
|
NP_000534.3:p.Tyr497Asp
|
|
NM_001007593.3:c.1486T>G
|
NP_001007594.2:p.Tyr496Asp
|
|
NM_001318087.2:c.1509T>G
|
NP_001305016.1:p.Val503=
|
|
NM_001318088.2:c.568T>G
|
NP_001305017.1:p.Tyr190Asp
|
|
NM_001365135.2:c.1357T>G
|
NP_001352064.1:p.Tyr453Asp
|
|
NR_027400.3:n.1442T>G
|
|
|
NR_134502.2:n.981T>G
|
|
|