ENST00000344921.11:c.-181G>T
|
ENSP00000340883.6:n.-181G>T
|
|
ENST00000407422.8:c.-181G>T
|
ENSP00000383984.3:n.-181G>T
|
|
ENST00000491967.2:n.10G>T
|
|
|
ENST00000644036.2:c.-181G>T
MANE Select
|
ENSP00000494049.2:n.-181G>T
|
|
ENST00000646421.1:n.12G>T
|
|
|
ENST00000647057.1:c.-181G>T
|
ENSP00000494757.1:n.-181G>T
|
|
ENST00000263121.11:c.-181G>T
|
ENSP00000263121.7:n.-181G>T
|
|
ENST00000344921.10:c.-181G>T
|
ENSP00000340883.6:n.-181G>T
|
|
ENST00000417137.5:c.-181G>T
|
ENSP00000388489.1:n.-181G>T
|
|
NM_001007468.1:c.-181G>T
|
NP_001007469.1:n.-181G>T
|
|
NM_003073.3:c.-181G>T , LRG_520t1:c.-181G>T
|
NP_003064.2:n.-181G>T
|
|
XM_011530345.1:c.-181G>T
|
XP_011528647.1:n.-181G>T
|
|
XM_011530346.1:c.-181G>T
|
XP_011528648.1:n.-181G>T
|
|
NM_001007468.2:c.-181G>T
|
NP_001007469.1:n.-181G>T
|
|
NM_001317946.1:c.-181G>T
|
NP_001304875.1:n.-181G>T
|
|
NM_001362877.1:c.-181G>T
|
NP_001349806.1:n.-181G>T
|
|
NM_003073.4:c.-181G>T
|
NP_003064.2:n.-181G>T
|
|
NM_001007468.3:c.-181G>T
|
NP_001007469.1:n.-181G>T
|
|
NM_001317946.2:c.-181G>T
|
NP_001304875.1:n.-181G>T
|
|
NM_001362877.2:c.-181G>T
|
NP_001349806.1:n.-181G>T
|
|
NM_003073.5:c.-181G>T
MANE Select
|
NP_003064.2:n.-181G>T
|
|