ENST00000433473.8:c.842T>C
|
ENSP00000394863.4:p.Phe281Ser
|
|
ENST00000439754.6:c.773T>C
|
ENSP00000403207.2:p.Phe258Ser
|
|
ENST00000449045.7:c.536T>C
|
ENSP00000392293.2:p.Phe179Ser
|
|
ENST00000527311.7:c.614T>C
|
ENSP00000436695.3:p.Phe205Ser
|
|
ENST00000530076.6:c.188T>C
|
ENSP00000434007.1:p.Phe63Ser
|
|
ENST00000530704.6:c.*468T>C
|
ENSP00000431655.1:n.*468T>C
|
|
ENST00000641083.1:c.935T>C
|
|
|
ENST00000641236.1:n.1082T>C
|
|
|
ENST00000641319.1:c.*55T>C
|
ENSP00000493128.1:n.*55T>C
|
|
ENST00000641381.1:c.267T>C
|
|
|
ENST00000641471.1:c.932T>C
|
ENSP00000493146.1:p.Phe311Ser
|
|
ENST00000641691.1:c.*697T>C
|
ENSP00000492910.1:n.*697T>C
|
|
ENST00000641924.1:c.*274T>C
|
ENSP00000493063.1:n.*274T>C
|
|
ENST00000642050.2:c.845T>C
MANE Select
|
ENSP00000493153.1:p.Phe282Ser
|
|
ENST00000372775.2:n.242T>C
|
|
|
ENST00000433473.7:c.845T>C
|
ENSP00000394863.3:p.Phe282Ser
|
|
ENST00000439754.5:c.458T>C
|
ENSP00000403207.1:p.Phe153Ser
|
|
ENST00000449045.6:c.536T>C
|
ENSP00000392293.2:p.Phe179Ser
|
|
ENST00000529905.5:c.845T>C
|
ENSP00000432053.1:p.Phe282Ser
|
|
ENST00000530076.5:c.188T>C
|
ENSP00000434007.1:p.Phe63Ser
|
|
ENST00000530704.5:c.*468T>C
|
ENSP00000431655.1:n.*468T>C
|
|
NM_000310.3:c.845T>C , LRG_690t1:c.845T>C
|
NP_000301.1:p.Phe282Ser
|
|
NM_001142604.1:c.536T>C
|
NP_001136076.1:p.Phe179Ser
|
|
XM_005271008.1:c.773T>C
|
XP_005271065.1:p.Phe258Ser
|
|
NM_001363695.1:c.773T>C
|
NP_001350624.1:p.Phe258Ser
|
|
NM_000310.4:c.845T>C
MANE Select
|
NP_000301.1:p.Phe282Ser
|
|
NM_001142604.2:c.536T>C
|
NP_001136076.1:p.Phe179Ser
|
|
NM_001363695.2:c.773T>C
|
NP_001350624.1:p.Phe258Ser
|
|