ENST00000342245.9:c.1731T>G
MANE Select
|
ENSP00000340409.4:p.His577Gln
|
|
ENST00000342245.8:c.1731T>G
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ENSP00000340409.4:p.His577Gln
|
|
ENST00000526280.1:c.788T>G
|
|
|
ENST00000527275.5:c.1728T>G
|
ENSP00000435350.1:p.His576Gln
|
|
ENST00000531303.5:c.*582T>G
|
ENSP00000432625.1:n.*582T>G
|
|
ENST00000533123.5:c.*458T>G
|
ENSP00000435950.1:n.*458T>G
|
|
ENST00000534405.5:c.*562T>G
|
ENSP00000434353.1:n.*562T>G
|
|
NM_000543.4:c.1731T>G
|
NP_000534.3:p.His577Gln
|
|
NM_001007593.2:c.1728T>G
|
NP_001007594.2:p.His576Gln
|
|
XM_005253075.3:c.*224T>G
|
XP_005253132.1:n.*224T>G
|
|
XM_011520303.1:c.1599T>G
|
XP_011518605.1:p.His533Gln
|
|
XM_011520304.1:c.*224T>G
|
XP_011518606.1:n.*224T>G
|
|
NM_001318087.1:c.*224T>G
|
NP_001305016.1:n.*224T>G
|
|
NM_001318088.1:c.810T>G
|
NP_001305017.1:p.His270Gln
|
|
NM_001365135.1:c.1599T>G
|
NP_001352064.1:p.His533Gln
|
|
NR_027400.2:n.1744T>G
|
|
|
NR_134502.1:n.1283T>G
|
|
|
XM_011520304.2:c.*224T>G
|
XP_011518606.1:n.*224T>G
|
|
XR_001747940.2:n.1916T>G
|
|
|
XR_002957158.1:n.2098T>G
|
|
|
NM_000543.5:c.1731T>G
MANE Select
|
NP_000534.3:p.His577Gln
|
|
NM_001007593.3:c.1728T>G
|
NP_001007594.2:p.His576Gln
|
|
NM_001318087.2:c.*224T>G
|
NP_001305016.1:n.*224T>G
|
|
NM_001318088.2:c.810T>G
|
NP_001305017.1:p.His270Gln
|
|
NM_001365135.2:c.1599T>G
|
NP_001352064.1:p.His533Gln
|
|
NR_027400.3:n.1684T>G
|
|
|
NR_134502.2:n.1223T>G
|
|
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