|
ENST00000647720.2:c.3517+105G>T
|
ENSP00000497673.2:n.3517+105G>T
|
|
|
ENST00000647978.2:c.*3336G>T
|
ENSP00000497658.1:n.*3336G>T
|
|
|
ENST00000649781.2:c.3439G>T
|
ENSP00000497203.1:p.Gly1147Cys
|
|
|
ENST00000685018.2:c.3622G>T
|
ENSP00000510194.2:p.Gly1208Cys
|
|
|
ENST00000687278.2:c.*275G>T
|
ENSP00000509593.2:n.*275G>T
|
|
|
ENST00000699585.1:c.3517+105G>T
|
ENSP00000514456.1:n.3517+105G>T
|
|
|
ENST00000699598.1:c.3622G>T
|
ENSP00000514467.1:p.Gly1208Cys
|
|
|
ENST00000699599.1:c.3622G>T
|
ENSP00000514468.1:p.Gly1208Cys
|
|
|
ENST00000699600.1:c.*283G>T
|
ENSP00000514469.1:n.*283G>T
|
|
|
ENST00000699601.1:c.*1997G>T
|
ENSP00000514470.1:n.*1997G>T
|
|
|
ENST00000699602.1:c.3616G>T
|
ENSP00000514471.1:p.Gly1206Cys
|
|
|
ENST00000699604.1:c.*3446G>T
|
ENSP00000514472.1:n.*3446G>T
|
|
|
ENST00000699605.1:c.3196G>T
|
ENSP00000514473.1:p.Gly1066Cys
|
|
|
ENST00000685018.1:c.370G>T
|
ENSP00000510194.1:p.Gly124Cys
|
|
|
ENST00000687278.1:c.1409G>T
|
ENSP00000509593.1:n.1409G>T
|
|
|
ENST00000689011.1:c.204G>T
|
|
|
|
ENST00000003084.11:c.3622G>T
MANE Select
|
ENSP00000003084.6:p.Gly1208Cys
|
|
|
ENST00000647720.1:c.1167+105G>T
|
|
|
|
ENST00000648260.1:c.2404G>T
|
ENSP00000497957.1:p.Gly802Cys
|
|
|
ENST00000649406.1:c.3439G>T
|
ENSP00000497965.1:p.Gly1147Cys
|
|
|
ENST00000649781.1:c.3439G>T
|
ENSP00000497203.1:p.Gly1147Cys
|
|
|
ENST00000003084.10:c.3622G>T
|
ENSP00000003084.6:p.Gly1208Cys
|
|
|
ENST00000426809.5:c.3532G>T
|
ENSP00000389119.1:p.Gly1178Cys
|
|
|
ENST00000468795.1:c.447G>T
|
|
|
|
NM_000492.3:c.3622G>T , LRG_663t1:c.3622G>T
|
NP_000483.3:p.Gly1208Cys
|
|
|
XM_011515751.1:c.3712G>T
|
XP_011514053.1:p.Gly1238Cys
|
|
|
XM_011515752.1:c.3712G>T
|
XP_011514054.1:p.Gly1238Cys
|
|
|
XM_011515753.1:c.3379G>T
|
XP_011514055.1:p.Gly1127Cys
|
|
|
XM_011515754.1:c.3379G>T
|
XP_011514056.1:p.Gly1127Cys
|
|
|
NM_000492.4:c.3622G>T
MANE Select
|
NP_000483.3:p.Gly1208Cys
|
|
