ENST00000265512.12:c.*87G>T
MANE Select
|
ENSP00000265512.7:n.*87G>T
|
|
ENST00000265512.11:c.*87G>T
|
ENSP00000265512.7:n.*87G>T
|
|
ENST00000508393.5:c.*87G>T
|
ENSP00000424630.1:n.*87G>T
|
|
ENST00000629236.2:c.*51G>T
|
ENSP00000486450.1:n.*51G>T
|
|
NM_000670.3:c.*87G>T
|
NP_000661.2:n.*87G>T
|
|
NM_000670.4:c.*87G>T
|
NP_000661.2:n.*87G>T
|
|
NM_001306171.1:c.*87G>T
|
NP_001293100.1:n.*87G>T
|
|
NM_001306172.1:c.*87G>T
|
NP_001293101.1:n.*87G>T
|
|
NR_037884.1:n.429-9200C>A
|
|
|
XR_938685.1:n.1569G>T
|
|
|
XR_938686.1:n.1560G>T
|
|
|
XR_938687.1:n.1433G>T
|
|
|
NM_000670.5:c.*87G>T
MANE Select
|
NP_000661.2:n.*87G>T
|
|
NM_001306171.2:c.*87G>T
|
NP_001293100.1:n.*87G>T
|
|
NM_001306172.2:c.*87G>T
|
NP_001293101.1:n.*87G>T
|
|