|
NM_001854.4:c.934G>A
MANE Select
|
NP_001845.3:p.Gly312Arg
|
|
ENST00000370096.9:c.934G>A
MANE Select
|
ENSP00000359114.3:p.Gly312Arg
|
|
NM_001190709.1:c.817G>A
|
NP_001177638.1:p.Gly273Arg
|
|
NM_001190709.2:c.817G>A
|
NP_001177638.1:p.Gly273Arg
|
|
NM_001854.3:c.934G>A
|
NP_001845.3:p.Gly312Arg
|
|
NM_080629.2:c.970G>A
|
NP_542196.2:p.Gly324Arg
|
|
NM_080629.3:c.970G>A
|
NP_542196.2:p.Gly324Arg
|
|
NM_080630.3:c.897+639G>A
|
NP_542197.3:n.897+639G>A
|
|
NM_080630.4:c.897+639G>A
|
NP_542197.3:n.897+639G>A
|
|
NR_134980.1:n.1252G>A
|
|
|
NR_134980.2:n.1278G>A
|
|
|
ENST00000353414.8:c.817G>A
|
ENSP00000302551.6:p.Gly273Arg
|
|
ENST00000358392.6:c.970G>A
|
ENSP00000351163.2:p.Gly324Arg
|
|
ENST00000370096.7:c.934G>A
|
ENSP00000359114.3:p.Gly312Arg
|
|
ENST00000427239.5:c.970G>A
|
ENSP00000408640.1:p.Gly324Arg
|
|
ENST00000461720.6:c.1087G>A
|
ENSP00000494909.1:p.Gly363Arg
|
|
ENST00000512756.5:c.897+639G>A
|
ENSP00000426533.1:n.897+639G>A
|
|
ENST00000635193.1:c.252G>A
|
|
|
ENST00000644186.1:c.934G>A
|
ENSP00000493821.1:p.Gly312Arg
|
|
ENST00000645458.1:c.934G>A
|
ENSP00000494179.1:p.Gly312Arg
|
|
ENST00000647280.1:c.934G>A
|
ENSP00000494583.1:p.Gly312Arg
|
|
XM_011540719.1:c.934G>A
|
XP_011539021.1:p.Gly312Arg
|
|
XM_011540721.1:c.-1495G>A
|
XP_011539023.1:n.-1495G>A
|
|
XM_017000334.1:c.1087G>A
|
XP_016855823.1:p.Gly363Arg
|
|
XM_017000335.1:c.1081G>A
|
XP_016855824.1:p.Gly361Arg
|
|
XM_017000336.1:c.1087G>A
|
XP_016855825.1:p.Gly363Arg
|
|
XR_946545.1:n.1332G>A
|
|