ENST00000343307.5:c.1065-77G>A
MANE Select
|
ENSP00000343002.4:n.1065-77G>A
|
|
ENST00000343307.4:c.1065-77G>A
|
ENSP00000343002.4:n.1065-77G>A
|
|
NM_194318.3:c.1065-77G>A
|
NP_919299.3:n.1065-77G>A
|
|
XM_006719768.2:c.1008-77G>A
|
XP_006719831.1:n.1008-77G>A
|
|
XM_011534936.1:c.1065-6262G>A
|
XP_011533238.1:n.1065-6262G>A
|
|
XM_011534937.1:c.945-77G>A
|
XP_011533239.1:n.945-77G>A
|
|
XM_011534938.1:c.918-77G>A
|
XP_011533240.1:n.918-77G>A
|
|
XR_941500.1:n.1250-77G>A
|
|
|
XR_941501.1:n.1130-77G>A
|
|
|
XM_006719768.3:c.1008-77G>A
|
XP_006719831.1:n.1008-77G>A
|
|
XM_011534938.2:c.918-77G>A
|
XP_011533240.1:n.918-77G>A
|
|
XM_017020395.1:c.918-77G>A
|
XP_016875884.1:n.918-77G>A
|
|
NM_194318.4:c.1065-77G>A
MANE Select
|
NP_919299.3:n.1065-77G>A
|
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