ENST00000342245.9:c.1091+334T>G
MANE Select
|
ENSP00000340409.4:n.1091+334T>G
|
|
ENST00000342245.8:c.1091+334T>G
|
ENSP00000340409.4:n.1091+334T>G
|
|
ENST00000526280.1:c.320+294T>G
|
|
|
ENST00000527275.5:c.1088+334T>G
|
ENSP00000435350.1:n.1088+334T>G
|
|
ENST00000531303.5:c.439-726T>G
|
ENSP00000432625.1:n.439-726T>G
|
|
ENST00000533123.5:c.1091+334T>G
|
ENSP00000435950.1:n.1091+334T>G
|
|
ENST00000534405.5:c.1131+294T>G
|
ENSP00000434353.1:n.1131+294T>G
|
|
NM_000543.4:c.1091+334T>G
|
NP_000534.3:n.1091+334T>G
|
|
NM_001007593.2:c.1088+334T>G
|
NP_001007594.2:n.1088+334T>G
|
|
XM_005253075.3:c.1091+334T>G
|
XP_005253132.1:n.1091+334T>G
|
|
XM_011520303.1:c.1131+294T>G
|
XP_011518605.1:n.1131+294T>G
|
|
XM_011520304.1:c.1131+294T>G
|
XP_011518606.1:n.1131+294T>G
|
|
XR_930886.1:n.1429+294T>G
|
|
|
NM_001318087.1:c.1091+334T>G
|
NP_001305016.1:n.1091+334T>G
|
|
NM_001318088.1:c.170+294T>G
|
NP_001305017.1:n.170+294T>G
|
|
NM_001365135.1:c.1131+294T>G
|
NP_001352064.1:n.1131+294T>G
|
|
NR_027400.2:n.1276+334T>G
|
|
|
NR_134502.1:n.624-726T>G
|
|
|
XM_011520304.2:c.1131+294T>G
|
XP_011518606.1:n.1131+294T>G
|
|
XR_001747940.2:n.1256+294T>G
|
|
|
XR_002957158.1:n.1256+294T>G
|
|
|
NM_000543.5:c.1091+334T>G
MANE Select
|
NP_000534.3:n.1091+334T>G
|
|
NM_001007593.3:c.1088+334T>G
|
NP_001007594.2:n.1088+334T>G
|
|
NM_001318087.2:c.1091+334T>G
|
NP_001305016.1:n.1091+334T>G
|
|
NM_001318088.2:c.170+294T>G
|
NP_001305017.1:n.170+294T>G
|
|
NM_001365135.2:c.1131+294T>G
|
NP_001352064.1:n.1131+294T>G
|
|
NR_027400.3:n.1216+334T>G
|
|
|
NR_134502.2:n.564-726T>G
|
|
|