|
ENST00000409134.8:c.986G>A
MANE Select
|
ENSP00000387123.3:p.Arg329Lys
|
|
|
ENST00000458249.6:c.*895G>A
|
ENSP00000403929.1:n.*895G>A
|
|
|
ENST00000497231.7:n.1413G>A
|
|
|
|
ENST00000503281.6:c.575G>A
|
|
|
|
ENST00000509459.6:c.495G>A
|
|
|
|
ENST00000635851.1:c.984G>A
|
|
|
|
ENST00000636062.1:n.881G>A
|
|
|
|
ENST00000636225.1:c.*930G>A
|
ENSP00000490797.1:n.*930G>A
|
|
|
ENST00000636286.1:n.704G>A
|
|
|
|
ENST00000636482.1:n.473G>A
|
|
|
|
ENST00000636743.1:c.866G>A
|
ENSP00000489725.1:p.Arg289Lys
|
|
|
ENST00000636808.1:c.*795G>A
|
ENSP00000490833.1:n.*795G>A
|
|
|
ENST00000636872.1:c.1146G>A
|
ENSP00000490919.1:n.1146G>A
|
|
|
ENST00000636879.1:c.1031G>A
|
ENSP00000490811.1:p.Arg344Lys
|
|
|
ENST00000636886.1:c.785G>A
|
ENSP00000490371.1:p.Arg262Lys
|
|
|
ENST00000637206.1:c.913+1821G>A
|
ENSP00000489895.1:n.913+1821G>A
|
|
|
ENST00000637272.1:c.977G>A
|
ENSP00000489686.1:p.Arg326Lys
|
|
|
ENST00000637292.1:c.559G>A
|
|
|
|
ENST00000637782.1:c.986G>A
|
ENSP00000490024.1:p.Arg329Lys
|
|
|
ENST00000637964.1:c.932G>A
|
ENSP00000490291.1:p.Arg311Lys
|
|
|
ENST00000638008.1:c.*830G>A
|
ENSP00000490400.1:n.*830G>A
|
|
|
ENST00000409134.7:c.986G>A
|
ENSP00000387123.3:p.Arg329Lys
|
|
|
ENST00000447989.6:c.1067G>A
|
ENSP00000414132.2:p.Arg356Lys
|
|
|
ENST00000497231.6:n.1196G>A
|
|
|
|
ENST00000503281.5:c.575G>A
|
|
|
|
ENST00000509459.5:c.495G>A
|
|
|
|
ENST00000553117.5:c.986G>A
|
ENSP00000448593.1:p.Arg329Lys
|
|
|
NM_001182.4:c.986G>A
|
NP_001173.2:p.Arg329Lys
|
|
|
NM_001201377.1:c.902G>A
|
NP_001188306.1:p.Arg301Lys
|
|
|
NM_001202404.1:c.1067G>A
|
NP_001189333.1:p.Arg356Lys
|
|
|
XM_011543417.1:c.581G>A
|
XP_011541719.1:p.Arg194Lys
|
|
|
XM_011543417.2:c.581G>A
|
XP_011541719.1:p.Arg194Lys
|
|
|
NM_001182.5:c.986G>A
MANE Select
|
NP_001173.2:p.Arg329Lys
|
|
|
NM_001201377.2:c.902G>A
|
NP_001188306.1:p.Arg301Lys
|
|
|
NM_001202404.2:c.986G>A
|
NP_001189333.2:p.Arg329Lys
|
|
