|
ENST00000647720.2:c.3386T>A
|
ENSP00000497673.2:p.Val1129Asp
|
|
|
ENST00000647978.2:c.*3100T>A
|
ENSP00000497658.1:n.*3100T>A
|
|
|
ENST00000649781.2:c.3203T>A
|
ENSP00000497203.1:p.Val1068Asp
|
|
|
ENST00000685018.2:c.3386T>A
|
ENSP00000510194.2:p.Val1129Asp
|
|
|
ENST00000687278.2:c.3386T>A
|
ENSP00000509593.2:p.Val1129Asp
|
|
|
ENST00000699585.1:c.3386T>A
|
ENSP00000514456.1:p.Val1129Asp
|
|
|
ENST00000699598.1:c.3386T>A
|
ENSP00000514467.1:p.Val1129Asp
|
|
|
ENST00000699599.1:c.3386T>A
|
ENSP00000514468.1:p.Val1129Asp
|
|
|
ENST00000699600.1:c.3386T>A
|
ENSP00000514469.1:p.Val1129Asp
|
|
|
ENST00000699601.1:c.*1761T>A
|
ENSP00000514470.1:n.*1761T>A
|
|
|
ENST00000699602.1:c.3380T>A
|
ENSP00000514471.1:p.Val1127Asp
|
|
|
ENST00000699604.1:c.*3210T>A
|
ENSP00000514472.1:n.*3210T>A
|
|
|
ENST00000699605.1:c.2960T>A
|
ENSP00000514473.1:p.Val987Asp
|
|
|
ENST00000685018.1:c.134T>A
|
ENSP00000510194.1:p.Val45Asp
|
|
|
ENST00000687278.1:c.977T>A
|
ENSP00000509593.1:p.Val326Asp
|
|
|
ENST00000003084.11:c.3386T>A
MANE Select
|
ENSP00000003084.6:p.Val1129Asp
|
|
|
ENST00000647720.1:c.1036T>A
|
|
|
|
ENST00000648260.1:c.2168T>A
|
ENSP00000497957.1:p.Val723Asp
|
|
|
ENST00000649406.1:c.3203T>A
|
ENSP00000497965.1:p.Val1068Asp
|
|
|
ENST00000649781.1:c.3203T>A
|
ENSP00000497203.1:p.Val1068Asp
|
|
|
ENST00000003084.10:c.3386T>A
|
ENSP00000003084.6:p.Val1129Asp
|
|
|
ENST00000426809.5:c.3296T>A
|
ENSP00000389119.1:p.Val1099Asp
|
|
|
ENST00000468795.1:c.211T>A
|
|
|
|
NM_000492.3:c.3386T>A , LRG_663t1:c.3386T>A
|
NP_000483.3:p.Val1129Asp
|
|
|
XM_011515751.1:c.3476T>A
|
XP_011514053.1:p.Val1159Asp
|
|
|
XM_011515752.1:c.3476T>A
|
XP_011514054.1:p.Val1159Asp
|
|
|
XM_011515753.1:c.3143T>A
|
XP_011514055.1:p.Val1048Asp
|
|
|
XM_011515754.1:c.3143T>A
|
XP_011514056.1:p.Val1048Asp
|
|
|
NM_000492.4:c.3386T>A
MANE Select
|
NP_000483.3:p.Val1129Asp
|
|
