ENST00000584880.6:c.*439T>C
|
ENSP00000464347.2:n.*439T>C
|
|
ENST00000703608.1:c.*759T>C
|
ENSP00000515392.1:n.*759T>C
|
|
ENST00000703609.1:c.*21T>C
|
ENSP00000515393.1:n.*21T>C
|
|
ENST00000703610.1:c.*519T>C
|
ENSP00000515394.1:n.*519T>C
|
|
ENST00000310144.11:c.*21T>C
MANE Select
|
ENSP00000310572.6:n.*21T>C
|
|
ENST00000310144.10:c.*21T>C
|
ENSP00000310572.6:n.*21T>C
|
|
ENST00000375812.8:c.*21T>C
|
ENSP00000364970.4:n.*21T>C
|
|
ENST00000578570.5:n.1652T>C
|
|
|
ENST00000579147.5:n.2557T>C
|
|
|
ENST00000580864.5:c.*21T>C
|
ENSP00000462495.1:n.*21T>C
|
|
ENST00000584657.1:n.547T>C
|
|
|
NM_001199163.1:c.*21T>C
|
NP_001186092.1:n.*21T>C
|
|
NM_002805.5:c.*21T>C
|
NP_002796.4:n.*21T>C
|
|
XM_006721980.1:c.*21T>C
|
XP_006722043.1:n.*21T>C
|
|
XR_934508.1:n.1331T>C
|
|
|
XM_024450840.1:c.*21T>C
|
XP_024306608.1:n.*21T>C
|
|
XM_024450841.1:c.*21T>C
|
XP_024306609.1:n.*21T>C
|
|
XR_934508.2:n.1318T>C
|
|
|
NM_002805.6:c.*21T>C
MANE Select
|
NP_002796.4:n.*21T>C
|
|
NM_001199163.2:c.*21T>C
|
NP_001186092.1:n.*21T>C
|
|