ENST00000350051.8:c.*238T>C
MANE Select
|
ENSP00000324180.4:n.*238T>C
|
|
ENST00000301633.8:c.*238T>C
|
ENSP00000301633.3:n.*238T>C
|
|
ENST00000350051.7:c.*238T>C
|
ENSP00000324180.4:n.*238T>C
|
|
ENST00000374948.6:c.*135T>C
|
ENSP00000364086.1:n.*135T>C
|
|
ENST00000589892.1:n.683T>C
|
|
|
NM_001012270.1:c.*135T>C
|
NP_001012270.1:n.*135T>C
|
|
NM_001012271.1:c.*238T>C
|
NP_001012271.1:n.*238T>C
|
|
NM_001168.2:c.*238T>C
|
NP_001159.2:n.*238T>C
|
|
XR_243654.3:n.869T>C
|
|
|
XR_934452.1:n.938T>C
|
|
|
XR_243654.5:n.869T>C
|
|
|
XR_934452.3:n.938T>C
|
|
|
NM_001168.3:c.*238T>C
MANE Select
|
NP_001159.2:n.*238T>C
|
|
NM_001012270.2:c.*135T>C
|
NP_001012270.1:n.*135T>C
|
|
NM_001012271.2:c.*238T>C
|
NP_001012271.1:n.*238T>C
|
|