|
ENST00000556394.2:c.812A>G
|
ENSP00000451967.2:p.His271Arg
|
|
|
ENST00000682247.1:c.1271A>G
|
ENSP00000507213.1:p.His424Arg
|
|
|
ENST00000682382.1:c.843A>G
|
|
|
|
ENST00000682395.1:n.1449A>G
|
|
|
|
ENST00000682459.1:n.974A>G
|
|
|
|
ENST00000682467.1:c.1271A>G
|
ENSP00000508062.1:p.His424Arg
|
|
|
ENST00000682706.1:n.48A>G
|
|
|
|
ENST00000682795.1:c.1271A>G
|
ENSP00000507574.1:p.His424Arg
|
|
|
ENST00000682895.1:n.987A>G
|
|
|
|
ENST00000682955.1:n.559A>G
|
|
|
|
ENST00000683188.1:c.1246A>G
|
|
|
|
ENST00000683328.1:c.264A>G
|
ENSP00000508096.1:n.264A>G
|
|
|
ENST00000683380.1:n.935A>G
|
|
|
|
ENST00000683828.1:c.980A>G
|
|
|
|
ENST00000684259.1:n.1122A>G
|
|
|
|
ENST00000684444.1:c.18A>G
|
|
|
|
ENST00000684549.1:n.822A>G
|
|
|
|
ENST00000261534.9:c.1271A>G
MANE Select
|
ENSP00000261534.4:p.His424Arg
|
|
|
ENST00000261534.8:c.1271A>G
|
ENSP00000261534.4:p.His424Arg
|
|
|
ENST00000452340.7:n.1294A>G
|
|
|
|
ENST00000553880.5:n.142A>G
|
|
|
|
ENST00000554767.5:n.2057A>G
|
|
|
|
ENST00000554884.5:n.263A>G
|
|
|
|
ENST00000556404.1:n.405A>G
|
|
|
|
ENST00000556851.1:n.307A>G
|
|
|
|
ENST00000557675.5:n.361A>G
|
|
|
|
NM_013382.5:c.1271A>G , LRG_844t1:c.1271A>G
|
NP_037514.2:p.His424Arg
|
|
|
XM_011536675.1:c.1271A>G
|
XP_011534977.1:p.His424Arg
|
|
|
XM_011536676.1:c.938A>G
|
XP_011534978.1:p.His313Arg
|
|
|
XM_011536677.1:c.812A>G
|
XP_011534979.1:p.His271Arg
|
|
|
XM_011536678.1:c.1271A>G
|
XP_011534980.1:p.His424Arg
|
|
|
XM_011536679.1:c.365A>G
|
XP_011534981.1:p.His122Arg
|
|
|
XR_943416.1:n.1474A>G
|
|
|
|
XM_011536675.2:c.1271A>G
|
XP_011534977.1:p.His424Arg
|
|
|
XM_011536676.2:c.938A>G
|
XP_011534978.1:p.His313Arg
|
|
|
XM_011536677.3:c.812A>G
|
XP_011534979.1:p.His271Arg
|
|
|
XR_001750279.1:n.1471A>G
|
|
|
|
XR_001750282.1:n.1924A>G
|
|
|
|
XR_943416.3:n.1472A>G
|
|
|
|
NM_013382.6:c.1271A>G
|
NP_037514.2:p.His424Arg
|
|
|
NM_013382.7:c.1271A>G
MANE Select
|
NP_037514.2:p.His424Arg
|
|
