ENST00000354546.10:c.*337T>C
MANE Select
|
ENSP00000346550.5:n.*337T>C
|
|
ENST00000354546.9:c.*337T>C
|
ENSP00000346550.5:n.*337T>C
|
|
ENST00000377751.9:c.*337T>C
|
ENSP00000366980.5:n.*337T>C
|
|
ENST00000522664.5:c.201-149T>C
|
|
|
ENST00000523714.5:c.*337T>C
|
ENSP00000430517.1:n.*337T>C
|
|
NM_001155.4:c.*337T>C
|
NP_001146.2:n.*337T>C
|
|
NM_001193544.1:c.*337T>C
|
NP_001180473.1:n.*337T>C
|
|
XM_005268432.3:c.*337T>C
|
XP_005268489.1:n.*337T>C
|
|
NM_001363114.1:c.*337T>C
|
NP_001350043.1:n.*337T>C
|
|
NM_001155.5:c.*337T>C
MANE Select
|
NP_001146.2:n.*337T>C
|
|
NM_001193544.2:c.*337T>C
|
NP_001180473.1:n.*337T>C
|
|
NM_001363114.2:c.*337T>C
|
NP_001350043.1:n.*337T>C
|
|