ENST00000646893.2:c.1039A>C
|
ENSP00000494249.2:p.Asn347His
|
|
ENST00000428343.6:c.700A>C
MANE Select
|
ENSP00000401536.1:p.Asn234His
|
|
ENST00000646446.1:c.913A>C
|
ENSP00000494216.1:p.Asn305His
|
|
ENST00000646893.1:c.826A>C
|
ENSP00000494249.1:p.Asn276His
|
|
ENST00000428343.5:c.700A>C
|
ENSP00000401536.1:p.Asn234His
|
|
ENST00000481179.5:c.*416A>C
|
ENSP00000422968.1:n.*416A>C
|
|
NM_001145664.1:c.700A>C
|
NP_001139136.1:p.Asn234His
|
|
XM_011511771.1:c.928A>C
|
XP_011510073.1:p.Asn310His
|
|
XM_011511772.1:c.913A>C
|
XP_011510074.1:p.Asn305His
|
|
XM_011511773.1:c.610A>C
|
XP_011510075.1:p.Asn204His
|
|
XM_011511774.1:c.928A>C
|
XP_011510076.1:p.Asn310His
|
|
XM_011511775.1:c.928A>C
|
XP_011510077.1:p.Asn310His
|
|
XM_011511776.1:c.412A>C
|
XP_011510078.1:p.Asn138His
|
|
XM_011511777.1:c.412A>C
|
XP_011510079.1:p.Asn138His
|
|
XM_011511778.1:c.412A>C
|
XP_011510080.1:p.Asn138His
|
|
XM_011511771.2:c.928A>C
|
XP_011510073.1:p.Asn310His
|
|
XM_011511777.2:c.412A>C
|
XP_011510079.1:p.Asn138His
|
|
XM_017004851.1:c.1039A>C
|
XP_016860340.1:p.Asn347His
|
|
XM_017004852.1:c.826A>C
|
XP_016860341.1:p.Asn276His
|
|
XM_017004853.1:c.1039A>C
|
XP_016860342.1:p.Asn347His
|
|
XM_017004854.1:c.1039A>C
|
XP_016860343.1:p.Asn347His
|
|
XR_001738924.1:n.983A>C
|
|
|
NM_001145664.2:c.700A>C
MANE Select
|
NP_001139136.2:p.Asn234His
|
|
NM_001367508.1:c.187A>C
|
NP_001354437.1:p.Asn63His
|
|
NM_001367509.1:c.187A>C
|
NP_001354438.1:p.Asn63His
|
|
NM_001367510.1:c.187A>C
|
NP_001354439.1:p.Asn63His
|
|