|
ENST00000342245.9:c.1152G>A
MANE Select
|
ENSP00000340409.4:p.Met384Ile
|
|
|
ENST00000342245.8:c.1152G>A
|
ENSP00000340409.4:p.Met384Ile
|
|
|
ENST00000526280.1:c.321-341G>A
|
|
|
|
ENST00000527275.5:c.1149G>A
|
ENSP00000435350.1:p.Met383Ile
|
|
|
ENST00000531303.5:c.499G>A
|
ENSP00000432625.1:p.Glu167Lys
|
|
|
ENST00000533123.5:c.1092-341G>A
|
ENSP00000435950.1:n.1092-341G>A
|
|
|
ENST00000534405.5:c.1192G>A
|
ENSP00000434353.1:p.Glu398Lys
|
|
|
NM_000543.4:c.1152G>A
|
NP_000534.3:p.Met384Ile
|
|
|
NM_001007593.2:c.1149G>A
|
NP_001007594.2:p.Met383Ile
|
|
|
XM_005253075.3:c.1152G>A
|
XP_005253132.1:p.Met384Ile
|
|
|
XM_011520303.1:c.1132-341G>A
|
XP_011518605.1:n.1132-341G>A
|
|
|
XM_011520304.1:c.1132-341G>A
|
XP_011518606.1:n.1132-341G>A
|
|
|
XR_930886.1:n.1490G>A
|
|
|
|
NM_001318087.1:c.1152G>A
|
NP_001305016.1:p.Met384Ile
|
|
|
NM_001318088.1:c.231G>A
|
NP_001305017.1:p.Met77Ile
|
|
|
NM_001365135.1:c.1132-341G>A
|
NP_001352064.1:n.1132-341G>A
|
|
|
NR_027400.2:n.1277-341G>A
|
|
|
|
NR_134502.1:n.684G>A
|
|
|
|
XM_011520304.2:c.1132-341G>A
|
XP_011518606.1:n.1132-341G>A
|
|
|
XR_001747940.2:n.1317G>A
|
|
|
|
XR_002957158.1:n.1317G>A
|
|
|
|
NM_000543.5:c.1152G>A
MANE Select
|
NP_000534.3:p.Met384Ile
|
|
|
NM_001007593.3:c.1149G>A
|
NP_001007594.2:p.Met383Ile
|
|
|
NM_001318087.2:c.1152G>A
|
NP_001305016.1:p.Met384Ile
|
|
|
NM_001318088.2:c.231G>A
|
NP_001305017.1:p.Met77Ile
|
|
|
NM_001365135.2:c.1132-341G>A
|
NP_001352064.1:n.1132-341G>A
|
|
|
NR_027400.3:n.1217-341G>A
|
|
|
|
NR_134502.2:n.624G>A
|
|
|
