ENST00000350721.9:c.6244T>G
MANE Select
|
ENSP00000343741.4:p.Phe2082Val
|
|
ENST00000513291.2:n.1428T>G
|
|
|
ENST00000654170.1:n.1087T>G
|
|
|
ENST00000656590.1:c.5034T>G
|
|
|
ENST00000661310.1:c.6052T>G
|
ENSP00000499589.1:p.Phe2018Val
|
|
ENST00000665483.1:n.99T>G
|
|
|
ENST00000666447.1:n.79T>G
|
|
|
ENST00000666943.1:n.1708T>G
|
|
|
ENST00000350721.8:c.6244T>G
|
ENSP00000343741.4:p.Phe2082Val
|
|
NM_001184.3:c.6244T>G
|
NP_001175.2:p.Phe2082Val
|
|
XM_011512924.1:c.6250T>G
|
XP_011511226.1:p.Phe2084Val
|
|
XM_011512925.1:c.6058T>G
|
XP_011511227.1:p.Phe2020Val
|
|
XR_924147.1:n.6339T>G
|
|
|
XR_924148.1:n.6339T>G
|
|
|
XR_924149.1:n.6218T>G
|
|
|
NM_001354579.1:c.6052T>G
|
NP_001341508.1:p.Phe2018Val
|
|
XR_001740179.2:n.6333T>G
|
|
|
XR_001740180.2:n.6387T>G
|
|
|
XR_001740181.2:n.6266T>G
|
|
|
XR_001740182.1:n.6218T>G
|
|
|
XR_002959543.1:n.6443T>G
|
|
|
XR_924148.2:n.6339T>G
|
|
|
NM_001184.4:c.6244T>G
MANE Select
|
NP_001175.2:p.Phe2082Val
|
|
NM_001354579.2:c.6052T>G
|
NP_001341508.1:p.Phe2018Val
|
|