|
ENST00000647720.2:c.3305G>C
|
ENSP00000497673.2:p.Arg1102Thr
|
|
|
ENST00000647978.2:c.*3019G>C
|
ENSP00000497658.1:n.*3019G>C
|
|
|
ENST00000649781.2:c.3122G>C
|
ENSP00000497203.1:p.Arg1041Thr
|
|
|
ENST00000685018.2:c.3305G>C
|
ENSP00000510194.2:p.Arg1102Thr
|
|
|
ENST00000687278.2:c.3305G>C
|
ENSP00000509593.2:p.Arg1102Thr
|
|
|
ENST00000699585.1:c.3305G>C
|
ENSP00000514456.1:p.Arg1102Thr
|
|
|
ENST00000699598.1:c.3305G>C
|
ENSP00000514467.1:p.Arg1102Thr
|
|
|
ENST00000699599.1:c.3305G>C
|
ENSP00000514468.1:p.Arg1102Thr
|
|
|
ENST00000699600.1:c.3305G>C
|
ENSP00000514469.1:p.Arg1102Thr
|
|
|
ENST00000699601.1:c.*1605G>C
|
ENSP00000514470.1:n.*1605G>C
|
|
|
ENST00000699602.1:c.3305G>C
|
ENSP00000514471.1:p.Arg1102Thr
|
|
|
ENST00000699604.1:c.*3129G>C
|
ENSP00000514472.1:n.*3129G>C
|
|
|
ENST00000699605.1:c.2879G>C
|
ENSP00000514473.1:p.Arg960Thr
|
|
|
ENST00000685018.1:c.53G>C
|
ENSP00000510194.1:p.Arg18Thr
|
|
|
ENST00000687278.1:c.896G>C
|
ENSP00000509593.1:p.Arg299Thr
|
|
|
ENST00000003084.11:c.3305G>C
MANE Select
|
ENSP00000003084.6:p.Arg1102Thr
|
|
|
ENST00000647720.1:c.955G>C
|
|
|
|
ENST00000648260.1:c.2087G>C
|
ENSP00000497957.1:p.Arg696Thr
|
|
|
ENST00000649406.1:c.3122G>C
|
ENSP00000497965.1:p.Arg1041Thr
|
|
|
ENST00000649781.1:c.3122G>C
|
ENSP00000497203.1:p.Arg1041Thr
|
|
|
ENST00000003084.10:c.3305G>C
|
ENSP00000003084.6:p.Arg1102Thr
|
|
|
ENST00000426809.5:c.3215G>C
|
ENSP00000389119.1:p.Arg1072Thr
|
|
|
ENST00000468795.1:c.130G>C
|
|
|
|
NM_000492.3:c.3305G>C , LRG_663t1:c.3305G>C
|
NP_000483.3:p.Arg1102Thr
|
|
|
XM_011515751.1:c.3395G>C
|
XP_011514053.1:p.Arg1132Thr
|
|
|
XM_011515752.1:c.3395G>C
|
XP_011514054.1:p.Arg1132Thr
|
|
|
XM_011515753.1:c.3062G>C
|
XP_011514055.1:p.Arg1021Thr
|
|
|
XM_011515754.1:c.3062G>C
|
XP_011514056.1:p.Arg1021Thr
|
|
|
NM_000492.4:c.3305G>C
MANE Select
|
NP_000483.3:p.Arg1102Thr
|
|
