|
NM_032119.4:c.15830G>A
MANE Select
|
NP_115495.3:p.Arg5277His
|
|
ENST00000405460.9:c.15830G>A
MANE Select
|
ENSP00000384582.2:p.Arg5277His
|
|
NM_032119.3:c.15830G>A
|
NP_115495.3:p.Arg5277His
|
|
NR_003149.1:n.15843G>A
|
|
|
NR_003149.2:n.15846G>A
|
|
|
ENST00000405460.6:c.15830G>A
|
ENSP00000384582.2:p.Arg5277His
|
|
ENST00000425867.2:c.2813G>A
|
ENSP00000392618.2:p.Arg938His
|
|
ENST00000425867.3:c.4784G>A
|
ENSP00000392618.3:p.Arg1595His
|
|
ENST00000638510.1:n.3097G>A
|
|
|
ENST00000639431.1:c.265+134881G>A
|
ENSP00000491057.1:n.265+134881G>A
|
|
ENST00000640407.1:c.2240G>A
|
ENSP00000491425.1:p.Arg747His
|
|
XM_011543675.1:c.15827G>A
|
XP_011541977.1:p.Arg5276His
|
|
XM_011543676.1:c.15749G>A
|
XP_011541978.1:p.Arg5250His
|
|
XM_011543677.1:c.13133G>A
|
XP_011541979.1:p.Arg4378His
|
|
XM_017009963.2:c.15851G>A
|
XP_016865452.1:p.Arg5284His
|
|
XM_017009964.2:c.15848G>A
|
XP_016865453.1:p.Arg5283His
|
|
XM_017009965.1:c.15848G>A
|
XP_016865454.1:p.Arg5283His
|
|
XM_017009966.2:c.15770G>A
|
XP_016865455.1:p.Arg5257His
|
|
XM_017009967.1:c.15755G>A
|
XP_016865456.1:p.Arg5252His
|
|
XM_017009968.2:c.15671G>A
|
XP_016865457.1:p.Arg5224His
|
|
XM_017009969.2:c.15851G>A
|
XP_016865458.1:p.Arg5284His
|
|
XM_017009972.1:c.8969G>A
|
XP_016865461.1:p.Arg2990His
|
|
XM_017009973.1:c.8948G>A
|
XP_016865462.1:p.Arg2983His
|