ENST00000350721.9:c.5558+376A>G
MANE Select
|
ENSP00000343741.4:n.5558+376A>G
|
|
ENST00000513291.2:n.742+376A>G
|
|
|
ENST00000653868.1:n.5587+376A>G
|
|
|
ENST00000656590.1:c.4348+376A>G
|
|
|
ENST00000661310.1:c.5366+376A>G
|
ENSP00000499589.1:n.5366+376A>G
|
|
ENST00000666943.1:n.1022+376A>G
|
|
|
ENST00000350721.8:c.5558+376A>G
|
ENSP00000343741.4:n.5558+376A>G
|
|
ENST00000507620.2:n.654+376A>G
|
|
|
ENST00000514393.5:n.241+376A>G
|
|
|
NM_001184.3:c.5558+376A>G
|
NP_001175.2:n.5558+376A>G
|
|
XM_011512924.1:c.5564+376A>G
|
XP_011511226.1:n.5564+376A>G
|
|
XM_011512925.1:c.5372+376A>G
|
XP_011511227.1:n.5372+376A>G
|
|
XM_011512926.1:c.5564+376A>G
|
XP_011511228.1:n.5564+376A>G
|
|
XM_011512927.1:c.5564+376A>G
|
XP_011511229.1:n.5564+376A>G
|
|
XR_924147.1:n.5653+376A>G
|
|
|
XR_924148.1:n.5653+376A>G
|
|
|
XR_924149.1:n.5653+376A>G
|
|
|
NM_001354579.1:c.5366+376A>G
|
NP_001341508.1:n.5366+376A>G
|
|
XR_001740179.2:n.5647+376A>G
|
|
|
XR_001740180.2:n.5653+376A>G
|
|
|
XR_001740181.2:n.5653+376A>G
|
|
|
XR_001740182.1:n.5653+376A>G
|
|
|
XR_002959543.1:n.5653+376A>G
|
|
|
XR_924148.2:n.5653+376A>G
|
|
|
NM_001184.4:c.5558+376A>G
MANE Select
|
NP_001175.2:n.5558+376A>G
|
|
NM_001354579.2:c.5366+376A>G
|
NP_001341508.1:n.5366+376A>G
|
|