ENST00000609686.4:c.*1344T>C
MANE Select
|
ENSP00000477455.1:n.*1344T>C
|
|
ENST00000637214.1:c.69+47164T>C
|
ENSP00000489997.1:n.69+47164T>C
|
|
ENST00000609686.3:c.*1344T>C
|
ENSP00000477455.1:n.*1344T>C
|
|
XM_005253351.2:c.*1344T>C
|
XP_005253408.1:n.*1344T>C
|
|
XM_011520628.1:c.*1344T>C
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XP_011518930.1:n.*1344T>C
|
|
XM_011520629.1:c.*1344T>C
|
XP_011518931.1:n.*1344T>C
|
|
XM_011520630.1:c.*1344T>C
|
XP_011518932.1:n.*1344T>C
|
|
NM_000834.4:c.*1344T>C
|
NP_000825.2:n.*1344T>C
|
|
XM_005253351.3:c.*1344T>C
|
XP_005253408.1:n.*1344T>C
|
|
XM_011520628.2:c.*1344T>C
|
XP_011518930.1:n.*1344T>C
|
|
XM_011520629.2:c.*1344T>C
|
XP_011518931.1:n.*1344T>C
|
|
XM_017019219.2:c.*1344T>C
|
XP_016874708.1:n.*1344T>C
|
|
NM_000834.5:c.*1344T>C
MANE Select
|
NP_000825.2:n.*1344T>C
|
|