ENST00000350721.9:c.7781A>G
MANE Select
|
ENSP00000343741.4:p.Asp2594Gly
|
|
ENST00000513291.2:n.6490A>G
|
|
|
ENST00000653893.1:n.2639A>G
|
|
|
ENST00000654170.1:n.2624A>G
|
|
|
ENST00000656114.1:n.2867A>G
|
|
|
ENST00000656590.1:c.6708A>G
|
|
|
ENST00000658083.1:n.2961A>G
|
|
|
ENST00000661310.1:c.7589A>G
|
ENSP00000499589.1:p.Asp2530Gly
|
|
ENST00000665483.1:n.5321A>G
|
|
|
ENST00000666447.1:n.4284A>G
|
|
|
ENST00000666943.1:n.4513A>G
|
|
|
ENST00000350721.8:c.7781A>G
|
ENSP00000343741.4:p.Asp2594Gly
|
|
ENST00000504521.5:c.370A>G
|
ENSP00000422553.1:n.370A>G
|
|
ENST00000513291.1:c.4845A>G
|
|
|
ENST00000515810.1:c.207A>G
|
ENSP00000421870.1:n.207A>G
|
|
NM_001184.3:c.7781A>G
|
NP_001175.2:p.Asp2594Gly
|
|
XM_011512924.1:c.7787A>G
|
XP_011511226.1:p.Asp2596Gly
|
|
XM_011512925.1:c.7595A>G
|
XP_011511227.1:p.Asp2532Gly
|
|
XR_924147.1:n.10538A>G
|
|
|
XR_924148.1:n.8013A>G
|
|
|
NM_001354579.1:c.7589A>G
|
NP_001341508.1:p.Asp2530Gly
|
|
XR_001740179.2:n.8007A>G
|
|
|
XR_924148.2:n.8013A>G
|
|
|
NM_001184.4:c.7781A>G
MANE Select
|
NP_001175.2:p.Asp2594Gly
|
|
NM_001354579.2:c.7589A>G
|
NP_001341508.1:p.Asp2530Gly
|
|