ENST00000350721.9:c.6552+17C>G
MANE Select
|
ENSP00000343741.4:n.6552+17C>G
|
|
ENST00000513291.2:n.1736+17C>G
|
|
|
ENST00000654170.1:n.1395+17C>G
|
|
|
ENST00000656590.1:c.5342+17C>G
|
|
|
ENST00000661310.1:c.6360+17C>G
|
ENSP00000499589.1:n.6360+17C>G
|
|
ENST00000665483.1:n.407+17C>G
|
|
|
ENST00000666447.1:n.404C>G
|
|
|
ENST00000666943.1:n.2033C>G
|
|
|
ENST00000350721.8:c.6552+17C>G
|
ENSP00000343741.4:n.6552+17C>G
|
|
ENST00000513291.1:c.91+17C>G
|
|
|
NM_001184.3:c.6552+17C>G
|
NP_001175.2:n.6552+17C>G
|
|
XM_011512924.1:c.6558+17C>G
|
XP_011511226.1:n.6558+17C>G
|
|
XM_011512925.1:c.6366+17C>G
|
XP_011511227.1:n.6366+17C>G
|
|
XR_924147.1:n.6647+17C>G
|
|
|
XR_924148.1:n.6647+17C>G
|
|
|
XR_924149.1:n.6526+17C>G
|
|
|
NM_001354579.1:c.6360+17C>G
|
NP_001341508.1:n.6360+17C>G
|
|
XR_001740179.2:n.6641+17C>G
|
|
|
XR_924148.2:n.6647+17C>G
|
|
|
NM_001184.4:c.6552+17C>G
MANE Select
|
NP_001175.2:n.6552+17C>G
|
|
NM_001354579.2:c.6360+17C>G
|
NP_001341508.1:n.6360+17C>G
|
|