ENST00000311469.9:c.404-41A>G
|
ENSP00000310873.4:n.404-41A>G
|
|
ENST00000647002.2:c.254-41A>G
MANE Select
|
ENSP00000495761.2:n.254-41A>G
|
|
ENST00000311461.7:c.254-41A>G
|
ENSP00000311835.7:n.254-41A>G
|
|
ENST00000311469.8:c.404-41A>G
|
ENSP00000310873.4:n.404-41A>G
|
|
ENST00000503391.5:c.254-41A>G
|
ENSP00000426242.1:n.254-41A>G
|
|
ENST00000514935.1:n.166-41A>G
|
|
|
NM_015697.7:c.404-41A>G
|
NP_056512.5:n.404-41A>G
|
|
XM_011531855.1:c.404-41A>G
|
XP_011530157.1:n.404-41A>G
|
|
XM_011531856.1:c.404-41A>G
|
XP_011530158.1:n.404-41A>G
|
|
XM_011531857.1:c.404-41A>G
|
XP_011530159.1:n.404-41A>G
|
|
XM_011531858.1:c.404-41A>G
|
XP_011530160.1:n.404-41A>G
|
|
XM_011531859.1:c.404-41A>G
|
XP_011530161.1:n.404-41A>G
|
|
XM_011531860.1:c.404-41A>G
|
XP_011530162.1:n.404-41A>G
|
|
XM_011531861.1:c.404-41A>G
|
XP_011530163.1:n.404-41A>G
|
|
XM_011531862.1:c.404-41A>G
|
XP_011530164.1:n.404-41A>G
|
|
XM_011531863.1:c.404-41A>G
|
XP_011530165.1:n.404-41A>G
|
|
XM_011531864.1:c.404-41A>G
|
XP_011530166.1:n.404-41A>G
|
|
XM_011531865.1:c.404-41A>G
|
XP_011530167.1:n.404-41A>G
|
|
XM_011531866.1:c.404-41A>G
|
XP_011530168.1:n.404-41A>G
|
|
XM_011531867.1:c.50-41A>G
|
XP_011530169.1:n.50-41A>G
|
|
XR_427543.2:n.563-41A>G
|
|
|
XR_938721.1:n.579-41A>G
|
|
|
NM_001358921.1:c.254-41A>G
|
NP_001345850.1:n.254-41A>G
|
|
NM_015697.8:c.404-41A>G
|
NP_056512.5:n.404-41A>G
|
|
XM_011531855.3:c.254-41A>G
|
XP_011530157.2:n.254-41A>G
|
|
XM_011531857.3:c.254-41A>G
|
XP_011530159.2:n.254-41A>G
|
|
XM_011531859.3:c.254-41A>G
|
XP_011530161.2:n.254-41A>G
|
|
XM_011531860.3:c.254-41A>G
|
XP_011530162.2:n.254-41A>G
|
|
XM_011531862.3:c.254-41A>G
|
XP_011530164.2:n.254-41A>G
|
|
XM_011531863.3:c.254-41A>G
|
XP_011530165.2:n.254-41A>G
|
|
XM_011531866.3:c.254-41A>G
|
XP_011530168.2:n.254-41A>G
|
|
XM_011531867.3:c.50-41A>G
|
XP_011530169.1:n.50-41A>G
|
|
XM_017008031.2:c.50-41A>G
|
XP_016863520.1:n.50-41A>G
|
|
XR_001741203.2:n.285-41A>G
|
|
|
XR_001741204.2:n.285-41A>G
|
|
|
XR_427543.4:n.285-41A>G
|
|
|
XR_938721.3:n.285-41A>G
|
|
|
NM_001358921.2:c.254-41A>G
MANE Select
|
NP_001345850.1:n.254-41A>G
|
|
NM_015697.9:c.404-41A>G
|
NP_056512.5:n.404-41A>G
|
|