ENST00000265512.12:c.*101C>A
MANE Select
|
ENSP00000265512.7:n.*101C>A
|
|
ENST00000265512.11:c.*101C>A
|
ENSP00000265512.7:n.*101C>A
|
|
ENST00000508393.5:c.*101C>A
|
ENSP00000424630.1:n.*101C>A
|
|
ENST00000629236.2:c.*65C>A
|
ENSP00000486450.1:n.*65C>A
|
|
NM_000670.3:c.*101C>A
|
NP_000661.2:n.*101C>A
|
|
NM_000670.4:c.*101C>A
|
NP_000661.2:n.*101C>A
|
|
NM_001306171.1:c.*101C>A
|
NP_001293100.1:n.*101C>A
|
|
NM_001306172.1:c.*101C>A
|
NP_001293101.1:n.*101C>A
|
|
NR_037884.1:n.429-9214G>T
|
|
|
XR_938685.1:n.1583C>A
|
|
|
XR_938686.1:n.1574C>A
|
|
|
XR_938687.1:n.1447C>A
|
|
|
NM_000670.5:c.*101C>A
MANE Select
|
NP_000661.2:n.*101C>A
|
|
NM_001306171.2:c.*101C>A
|
NP_001293100.1:n.*101C>A
|
|
NM_001306172.2:c.*101C>A
|
NP_001293101.1:n.*101C>A
|
|