ENST00000681687.1:c.-161-9902A>G
MANE Select
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ENSP00000505796.1:n.-161-9902A>G
|
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ENST00000400314.5:c.-126+10086A>G
|
ENSP00000383168.1:n.-126+10086A>G
|
|
ENST00000465077.5:n.286+10086A>G
|
|
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ENST00000593338.1:n.39-3866A>G
|
|
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ENST00000594149.5:n.326+1178A>G
|
|
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ENST00000628776.2:n.177+1178A>G
|
|
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NM_001348238.1:c.-161-9902A>G
|
NP_001335167.1:n.-161-9902A>G
|
|
NM_001348239.1:c.-161-9902A>G
|
NP_001335168.1:n.-161-9902A>G
|
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NM_001348240.1:c.-161-9902A>G
|
NP_001335169.1:n.-161-9902A>G
|
|
NM_001348241.1:c.-161-9902A>G
|
NP_001335170.1:n.-161-9902A>G
|
|
NM_001348242.1:c.-352-9902A>G
|
NP_001335171.1:n.-352-9902A>G
|
|
NR_145492.1:n.118-9902A>G
|
|
|
XM_024452086.1:c.-511-3866A>G
|
XP_024307854.1:n.-511-3866A>G
|
|
XM_024452087.1:c.-559-3866A>G
|
XP_024307855.1:n.-559-3866A>G
|
|
XM_024452088.1:c.-220-3866A>G
|
XP_024307856.1:n.-220-3866A>G
|
|
XM_024452089.1:c.-126+76563A>G
|
XP_024307857.1:n.-126+76563A>G
|
|
XM_024452090.1:c.-528-3866A>G
|
XP_024307858.1:n.-528-3866A>G
|
|
XM_024452091.1:c.-433-3866A>G
|
XP_024307859.1:n.-433-3866A>G
|
|
XM_024452117.1:c.-352-9902A>G
|
XP_024307885.1:n.-352-9902A>G
|
|
XM_024452118.1:c.-374-9902A>G
|
XP_024307886.1:n.-374-9902A>G
|
|
NM_001348238.2:c.-161-9902A>G
|
NP_001335167.1:n.-161-9902A>G
|
|
NM_001348239.2:c.-161-9902A>G
|
NP_001335168.1:n.-161-9902A>G
|
|
NM_001348240.2:c.-161-9902A>G
|
NP_001335169.1:n.-161-9902A>G
|
|
NM_001348241.2:c.-161-9902A>G
|
NP_001335170.1:n.-161-9902A>G
|
|
NM_001348242.2:c.-352-9902A>G
|
NP_001335171.1:n.-352-9902A>G
|
|
NM_001382276.1:c.-374-9902A>G
|
NP_001369205.1:n.-374-9902A>G
|
|
NM_001382281.1:c.-126+101647A>G
|
NP_001369210.1:n.-126+101647A>G
|
|
NM_001382282.1:c.-126+76563A>G
|
NP_001369211.1:n.-126+76563A>G
|
|
NM_001382283.1:c.-161-9902A>G
|
NP_001369212.1:n.-161-9902A>G
|
|
NM_001382284.1:c.-161-9902A>G
|
NP_001369213.1:n.-161-9902A>G
|
|
NM_001382285.1:c.-126+10086A>G
|
NP_001369214.1:n.-126+10086A>G
|
|
NM_001382286.1:c.-126+10086A>G
|
NP_001369215.1:n.-126+10086A>G
|
|
NM_001382287.1:c.-126+10086A>G
|
NP_001369216.1:n.-126+10086A>G
|
|
NM_001382288.1:c.-161-9902A>G
|
NP_001369217.1:n.-161-9902A>G
|
|
NM_001384156.1:c.-161-9902A>G
MANE Select
|
NP_001371085.1:n.-161-9902A>G
|
|
NR_145492.2:n.262-9902A>G
|
|
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