|
NM_032119.4:c.6815G>C
MANE Select
|
NP_115495.3:p.Trp2272Ser
|
|
ENST00000405460.9:c.6815G>C
MANE Select
|
ENSP00000384582.2:p.Trp2272Ser
|
|
NM_032119.3:c.6815G>C
|
NP_115495.3:p.Trp2272Ser
|
|
NR_003149.1:n.6911G>C
|
|
|
NR_003149.2:n.6914G>C
|
|
|
ENST00000405460.6:c.6815G>C
|
ENSP00000384582.2:p.Trp2272Ser
|
|
ENST00000639431.1:c.265+14696G>C
|
ENSP00000491057.1:n.265+14696G>C
|
|
ENST00000639473.1:n.2274G>C
|
|
|
ENST00000640012.1:c.705G>C
|
|
|
ENST00000640403.1:c.4106G>C
|
ENSP00000492531.1:p.Trp1369Ser
|
|
ENST00000640779.1:c.1627G>C
|
|
|
XM_011543675.1:c.6812G>C
|
XP_011541977.1:p.Trp2271Ser
|
|
XM_011543676.1:c.6734G>C
|
XP_011541978.1:p.Trp2245Ser
|
|
XM_011543677.1:c.4118G>C
|
XP_011541979.1:p.Trp1373Ser
|
|
XM_011543678.1:c.6815G>C
|
XP_011541980.1:p.Trp2272Ser
|
|
XM_011543679.1:c.6815G>C
|
XP_011541981.1:p.Trp2272Ser
|
|
XM_017009963.2:c.6815G>C
|
XP_016865452.1:p.Trp2272Ser
|
|
XM_017009964.2:c.6812G>C
|
XP_016865453.1:p.Trp2271Ser
|
|
XM_017009965.1:c.6812G>C
|
XP_016865454.1:p.Trp2271Ser
|
|
XM_017009966.2:c.6734G>C
|
XP_016865455.1:p.Trp2245Ser
|
|
XM_017009967.1:c.6719G>C
|
XP_016865456.1:p.Trp2240Ser
|
|
XM_017009968.2:c.6815G>C
|
XP_016865457.1:p.Trp2272Ser
|
|
XM_017009969.2:c.6815G>C
|
XP_016865458.1:p.Trp2272Ser
|
|
XM_017009970.2:c.6815G>C
|
XP_016865459.1:p.Trp2272Ser
|
|
XM_017009971.2:c.6815G>C
|
XP_016865460.1:p.Trp2272Ser
|
|
XM_017009972.1:c.16G>C
|
XP_016865461.1:p.Gly6Arg
|
|
XM_017009973.1:c.16G>C
|
XP_016865462.1:p.Gly6Arg
|
|
XM_017009974.2:c.6815G>C
|
XP_016865463.1:p.Trp2272Ser
|