ENST00000319555.8:c.269-11964T>C
MANE Select
|
ENSP00000326630.2:n.269-11964T>C
|
|
ENST00000319555.7:c.269-11964T>C
|
ENSP00000326630.2:n.269-11964T>C
|
|
ENST00000562437.2:c.269-11964T>C
|
ENSP00000480412.1:n.269-11964T>C
|
|
ENST00000563351.5:c.146-11964T>C
|
ENSP00000484216.1:n.146-11964T>C
|
|
ENST00000569086.5:c.269-11964T>C
|
ENSP00000482796.1:n.269-11964T>C
|
|
NM_153813.2:c.269-11964T>C
|
NP_722520.2:n.269-11964T>C
|
|
XM_011522912.1:c.407-11964T>C
|
XP_011521214.1:n.407-11964T>C
|
|
XM_011522913.1:c.516+13270T>C
|
XP_011521215.1:n.516+13270T>C
|
|
XM_011522914.1:c.368-11964T>C
|
XP_011521216.1:n.368-11964T>C
|
|
XM_011522915.1:c.233-11964T>C
|
XP_011521217.1:n.233-11964T>C
|
|
XM_011522916.1:c.315+13270T>C
|
XP_011521218.1:n.315+13270T>C
|
|
XM_011522918.1:c.215-11964T>C
|
XP_011521220.1:n.215-11964T>C
|
|
XM_011522912.2:c.407-11964T>C
|
XP_011521214.1:n.407-11964T>C
|
|
XM_011522914.2:c.368-11964T>C
|
XP_011521216.1:n.368-11964T>C
|
|
XM_017022982.1:c.7+11949T>C
|
XP_016878471.1:n.7+11949T>C
|
|
NM_153813.3:c.269-11964T>C
MANE Select
|
NP_722520.2:n.269-11964T>C
|
|