ENST00000350721.9:c.6504T>G
MANE Select
|
ENSP00000343741.4:p.Phe2168Leu
|
|
ENST00000513291.2:n.1688T>G
|
|
|
ENST00000654170.1:n.1347T>G
|
|
|
ENST00000656590.1:c.5294T>G
|
|
|
ENST00000661310.1:c.6312T>G
|
ENSP00000499589.1:p.Phe2104Leu
|
|
ENST00000665483.1:n.359T>G
|
|
|
ENST00000666447.1:n.339T>G
|
|
|
ENST00000666943.1:n.1968T>G
|
|
|
ENST00000350721.8:c.6504T>G
|
ENSP00000343741.4:p.Phe2168Leu
|
|
ENST00000513291.1:c.43T>G
|
|
|
NM_001184.3:c.6504T>G
|
NP_001175.2:p.Phe2168Leu
|
|
XM_011512924.1:c.6510T>G
|
XP_011511226.1:p.Phe2170Leu
|
|
XM_011512925.1:c.6318T>G
|
XP_011511227.1:p.Phe2106Leu
|
|
XR_924147.1:n.6599T>G
|
|
|
XR_924148.1:n.6599T>G
|
|
|
XR_924149.1:n.6478T>G
|
|
|
NM_001354579.1:c.6312T>G
|
NP_001341508.1:p.Phe2104Leu
|
|
XR_001740179.2:n.6593T>G
|
|
|
XR_924148.2:n.6599T>G
|
|
|
NM_001184.4:c.6504T>G
MANE Select
|
NP_001175.2:p.Phe2168Leu
|
|
NM_001354579.2:c.6312T>G
|
NP_001341508.1:p.Phe2104Leu
|
|