ENST00000406846.7:c.-29G>C
MANE Select
|
ENSP00000384708.2:n.-29G>C
|
|
ENST00000304421.8:c.-29G>C
|
ENSP00000306780.4:n.-29G>C
|
|
ENST00000406846.6:c.-29G>C
|
ENSP00000384708.2:n.-29G>C
|
|
ENST00000419927.1:c.-29G>C
|
ENSP00000405775.1:n.-29G>C
|
|
NM_000145.3:c.-29G>C , LRG_536t1:c.-29G>C
|
NP_000136.2:n.-29G>C
|
|
NM_181446.2:c.-29G>C
|
NP_852111.2:n.-29G>C
|
|
XM_011532733.1:c.-29G>C
|
XP_011531035.1:n.-29G>C
|
|
XM_011532734.1:c.-613G>C
|
XP_011531036.1:n.-613G>C
|
|
XM_011532737.1:c.-29G>C
|
XP_011531039.1:n.-29G>C
|
|
XM_011532738.1:c.-29G>C
|
XP_011531040.1:n.-29G>C
|
|
XM_011532739.1:c.-29G>C
|
XP_011531041.1:n.-29G>C
|
|
XM_011532740.1:c.-29G>C
|
XP_011531042.1:n.-29G>C
|
|
XM_011532733.2:c.-29G>C
|
XP_011531035.1:n.-29G>C
|
|
XM_011532734.2:c.-613G>C
|
XP_011531036.1:n.-613G>C
|
|
NM_000145.4:c.-29G>C
MANE Select
|
NP_000136.2:n.-29G>C
|
|
NM_181446.3:c.-29G>C
|
NP_852111.2:n.-29G>C
|
|