ENST00000265512.12:c.*9G>C
MANE Select
|
ENSP00000265512.7:n.*9G>C
|
|
ENST00000265512.11:c.*9G>C
|
ENSP00000265512.7:n.*9G>C
|
|
ENST00000505590.5:c.*9G>C
|
ENSP00000425416.1:n.*9G>C
|
|
ENST00000508393.5:c.*9G>C
|
ENSP00000424630.1:n.*9G>C
|
|
ENST00000509471.5:c.506G>C
|
ENSP00000424583.1:n.506G>C
|
|
ENST00000629236.2:c.1149G>C
|
ENSP00000486450.1:p.Gln383His
|
|
NM_000670.3:c.*9G>C
|
NP_000661.2:n.*9G>C
|
|
NM_000670.4:c.*9G>C
|
NP_000661.2:n.*9G>C
|
|
NM_001306171.1:c.*9G>C
|
NP_001293100.1:n.*9G>C
|
|
NM_001306172.1:c.*9G>C
|
NP_001293101.1:n.*9G>C
|
|
NR_037884.1:n.429-9122C>G
|
|
|
XR_938685.1:n.1491G>C
|
|
|
XR_938686.1:n.1482G>C
|
|
|
XR_938687.1:n.1355G>C
|
|
|
NM_000670.5:c.*9G>C
MANE Select
|
NP_000661.2:n.*9G>C
|
|
NM_001306171.2:c.*9G>C
|
NP_001293100.1:n.*9G>C
|
|
NM_001306172.2:c.*9G>C
|
NP_001293101.1:n.*9G>C
|
|