|
ENST00000647720.2:c.3379G>C
|
ENSP00000497673.2:p.Gly1127Arg
|
|
|
ENST00000647978.2:c.*3093G>C
|
ENSP00000497658.1:n.*3093G>C
|
|
|
ENST00000649781.2:c.3196G>C
|
ENSP00000497203.1:p.Gly1066Arg
|
|
|
ENST00000685018.2:c.3379G>C
|
ENSP00000510194.2:p.Gly1127Arg
|
|
|
ENST00000687278.2:c.3379G>C
|
ENSP00000509593.2:p.Gly1127Arg
|
|
|
ENST00000699585.1:c.3379G>C
|
ENSP00000514456.1:p.Gly1127Arg
|
|
|
ENST00000699598.1:c.3379G>C
|
ENSP00000514467.1:p.Gly1127Arg
|
|
|
ENST00000699599.1:c.3379G>C
|
ENSP00000514468.1:p.Gly1127Arg
|
|
|
ENST00000699600.1:c.3379G>C
|
ENSP00000514469.1:p.Gly1127Arg
|
|
|
ENST00000699601.1:c.*1754G>C
|
ENSP00000514470.1:n.*1754G>C
|
|
|
ENST00000699602.1:c.3373G>C
|
ENSP00000514471.1:p.Gly1125Arg
|
|
|
ENST00000699604.1:c.*3203G>C
|
ENSP00000514472.1:n.*3203G>C
|
|
|
ENST00000699605.1:c.2953G>C
|
ENSP00000514473.1:p.Gly985Arg
|
|
|
ENST00000685018.1:c.127G>C
|
ENSP00000510194.1:p.Gly43Arg
|
|
|
ENST00000687278.1:c.970G>C
|
ENSP00000509593.1:p.Gly324Arg
|
|
|
ENST00000003084.11:c.3379G>C
MANE Select
|
ENSP00000003084.6:p.Gly1127Arg
|
|
|
ENST00000647720.1:c.1029G>C
|
|
|
|
ENST00000648260.1:c.2161G>C
|
ENSP00000497957.1:p.Gly721Arg
|
|
|
ENST00000649406.1:c.3196G>C
|
ENSP00000497965.1:p.Gly1066Arg
|
|
|
ENST00000649781.1:c.3196G>C
|
ENSP00000497203.1:p.Gly1066Arg
|
|
|
ENST00000003084.10:c.3379G>C
|
ENSP00000003084.6:p.Gly1127Arg
|
|
|
ENST00000426809.5:c.3289G>C
|
ENSP00000389119.1:p.Gly1097Arg
|
|
|
ENST00000468795.1:c.204G>C
|
|
|
|
NM_000492.3:c.3379G>C , LRG_663t1:c.3379G>C
|
NP_000483.3:p.Gly1127Arg
|
|
|
XM_011515751.1:c.3469G>C
|
XP_011514053.1:p.Gly1157Arg
|
|
|
XM_011515752.1:c.3469G>C
|
XP_011514054.1:p.Gly1157Arg
|
|
|
XM_011515753.1:c.3136G>C
|
XP_011514055.1:p.Gly1046Arg
|
|
|
XM_011515754.1:c.3136G>C
|
XP_011514056.1:p.Gly1046Arg
|
|
|
NM_000492.4:c.3379G>C
MANE Select
|
NP_000483.3:p.Gly1127Arg
|
|
