|
ENST00000506455.6:c.1933A>C
MANE Select
|
ENSP00000424361.1:p.Asn645His
|
|
|
ENST00000296518.11:c.1933A>C
|
ENSP00000296518.7:p.Asn645His
|
|
|
ENST00000393832.7:c.1159A>C
|
ENSP00000377418.3:p.Asn387His
|
|
|
ENST00000443668.6:c.*1376A>C
|
ENSP00000409903.2:n.*1376A>C
|
|
|
ENST00000455639.6:c.1933A>C
|
ENSP00000412201.2:p.Asn645His
|
|
|
ENST00000506455.5:c.1933A>C
|
ENSP00000424361.1:p.Asn645His
|
|
|
ENST00000509901.5:c.*305A>C
|
ENSP00000424863.1:n.*305A>C
|
|
|
ENST00000511108.5:c.1933A>C
|
ENSP00000421493.1:p.Asn645His
|
|
|
ENST00000513574.1:c.1933A>C
|
ENSP00000426040.1:p.Asn645His
|
|
|
ENST00000515201.5:c.*305A>C
|
ENSP00000422141.1:n.*305A>C
|
|
|
ENST00000621234.4:c.*305A>C
|
ENSP00000479710.1:n.*305A>C
|
|
|
NM_000856.5:c.1933A>C
|
NP_000847.2:p.Asn645His
|
|
|
NM_001130682.2:c.1933A>C
|
NP_001124154.1:p.Asn645His
|
|
|
NM_001130683.3:c.1933A>C
|
NP_001124155.1:p.Asn645His
|
|
|
NM_001130684.2:c.1933A>C
|
NP_001124156.1:p.Asn645His
|
|
|
NM_001130685.2:c.1228A>C
|
NP_001124157.1:p.Asn410His
|
|
|
NM_001256449.1:c.1933A>C
|
NP_001243378.1:p.Asn645His
|
|
|
XM_005262955.1:c.1933A>C
|
XP_005263012.1:p.Asn645His
|
|
|
XM_005262956.1:c.1228A>C
|
XP_005263013.1:p.Asn410His
|
|
|
XM_005262957.1:c.1228A>C
|
XP_005263014.1:p.Asn410His
|
|
|
XM_006714196.1:c.1933A>C
|
XP_006714259.1:p.Asn645His
|
|
|
XM_006714197.1:c.1933A>C
|
XP_006714260.1:p.Asn645His
|
|
|
XM_006714198.1:c.1228A>C
|
XP_006714261.1:p.Asn410His
|
|
|
XM_011531899.1:c.1933A>C
|
XP_011530201.1:p.Asn645His
|
|
|
XM_011531900.1:c.1228A>C
|
XP_011530202.1:p.Asn410His
|
|
|
XR_939379.1:n.1262-2056T>G
|
|
|
|
XR_939380.1:n.1262-2056T>G
|
|
|
|
XR_939381.1:n.1262-2115T>G
|
|
|
|
XR_939382.1:n.1085-2056T>G
|
|
|
|
XR_939383.1:n.670-2056T>G
|
|
|
|
XR_939384.1:n.1262-2056T>G
|
|
|
|
XR_939385.1:n.578-2056T>G
|
|
|
|
XR_939386.1:n.1262-2056T>G
|
|
|
|
XR_939387.1:n.1262-2056T>G
|
|
|
|
XR_939388.1:n.1262-2056T>G
|
|
|
|
XM_005262955.3:c.1933A>C
|
XP_005263012.1:p.Asn645His
|
|
|
XM_005262956.3:c.1228A>C
|
XP_005263013.1:p.Asn410His
|
|
|
XM_005262957.3:c.1228A>C
|
XP_005263014.1:p.Asn410His
|
|
|
XM_006714196.2:c.1933A>C
|
XP_006714259.1:p.Asn645His
|
|
|
XM_006714197.2:c.1933A>C
|
XP_006714260.1:p.Asn645His
|
|
|
XM_011531900.2:c.1228A>C
|
XP_011530202.1:p.Asn410His
|
|
|
XR_001741896.1:n.2539-2115T>G
|
|
|
|
XR_001741897.1:n.2525-2115T>G
|
|
|
|
XR_001741898.1:n.1281-2115T>G
|
|
|
|
XR_001741899.1:n.689-2115T>G
|
|
|
|
NM_000856.6:c.1933A>C
|
NP_000847.2:p.Asn645His
|
|
|
NM_001130682.3:c.1933A>C
MANE Select
|
NP_001124154.1:p.Asn645His
|
|
|
NM_001130683.4:c.1933A>C
|
NP_001124155.1:p.Asn645His
|
|
|
NM_001130684.3:c.1933A>C
|
NP_001124156.1:p.Asn645His
|
|
|
NM_001130685.3:c.1228A>C
|
NP_001124157.1:p.Asn410His
|
|
|
NM_001256449.2:c.1933A>C
|
NP_001243378.1:p.Asn645His
|
|
|
NM_001379666.1:c.1933A>C
|
NP_001366595.1:p.Asn645His
|
|
|
NM_001379667.1:c.1933A>C
|
NP_001366596.1:p.Asn645His
|
|
|
NM_001379668.1:c.1933A>C
|
NP_001366597.1:p.Asn645His
|
|
|
NM_001379669.1:c.1933A>C
|
NP_001366598.1:p.Asn645His
|
|
|
NM_001379670.1:c.1933A>C
|
NP_001366599.1:p.Asn645His
|
|
|
NM_001379671.1:c.1933A>C
|
NP_001366600.1:p.Asn645His
|
|
|
NM_001379672.1:c.1933A>C
|
NP_001366601.1:p.Asn645His
|
|
|
NM_001379673.1:c.1933A>C
|
NP_001366602.1:p.Asn645His
|
|
|
NM_001379674.1:c.1933A>C
|
NP_001366603.1:p.Asn645His
|
|
|
NM_001379675.1:c.1778A>C
|
NP_001366604.1:p.Lys593Thr
|
|
|
NM_001379676.1:c.1426A>C
|
NP_001366605.1:p.Asn476His
|
|
