ENST00000350721.9:c.6552+44A>G
MANE Select
|
ENSP00000343741.4:n.6552+44A>G
|
|
ENST00000513291.2:n.1736+44A>G
|
|
|
ENST00000654170.1:n.1395+44A>G
|
|
|
ENST00000656590.1:c.5342+44A>G
|
|
|
ENST00000661310.1:c.6360+44A>G
|
ENSP00000499589.1:n.6360+44A>G
|
|
ENST00000665483.1:n.407+44A>G
|
|
|
ENST00000666447.1:n.431A>G
|
|
|
ENST00000666943.1:n.2060A>G
|
|
|
ENST00000350721.8:c.6552+44A>G
|
ENSP00000343741.4:n.6552+44A>G
|
|
ENST00000513291.1:c.91+44A>G
|
|
|
NM_001184.3:c.6552+44A>G
|
NP_001175.2:n.6552+44A>G
|
|
XM_011512924.1:c.6558+44A>G
|
XP_011511226.1:n.6558+44A>G
|
|
XM_011512925.1:c.6366+44A>G
|
XP_011511227.1:n.6366+44A>G
|
|
XR_924147.1:n.6647+44A>G
|
|
|
XR_924148.1:n.6647+44A>G
|
|
|
XR_924149.1:n.6526+44A>G
|
|
|
NM_001354579.1:c.6360+44A>G
|
NP_001341508.1:n.6360+44A>G
|
|
XR_001740179.2:n.6641+44A>G
|
|
|
XR_924148.2:n.6647+44A>G
|
|
|
NM_001184.4:c.6552+44A>G
MANE Select
|
NP_001175.2:n.6552+44A>G
|
|
NM_001354579.2:c.6360+44A>G
|
NP_001341508.1:n.6360+44A>G
|
|