ENST00000369409.9:c.499T>G
|
ENSP00000358417.5:p.Phe167Val
|
|
ENST00000462324.2:n.582T>G
|
|
|
ENST00000641023.2:c.499T>G
MANE Select
|
ENSP00000493175.1:p.Phe167Val
|
|
ENST00000641074.1:c.499T>G
|
ENSP00000493446.1:p.Phe167Val
|
|
ENST00000641115.1:c.499T>G
|
ENSP00000493264.1:p.Phe167Val
|
|
ENST00000641213.1:c.*152T>G
|
ENSP00000493079.1:n.*152T>G
|
|
ENST00000641247.1:c.*218T>G
|
ENSP00000492955.1:n.*218T>G
|
|
ENST00000641272.1:c.433T>G
|
ENSP00000493432.1:p.Phe145Val
|
|
ENST00000641314.1:n.484T>G
|
|
|
ENST00000641371.1:c.413T>G
|
ENSP00000493305.1:p.Leu138Arg
|
|
ENST00000641375.1:c.*335T>G
|
ENSP00000493089.1:n.*335T>G
|
|
ENST00000641455.1:n.44T>G
|
|
|
ENST00000641491.1:c.*152T>G
|
ENSP00000493187.1:n.*152T>G
|
|
ENST00000641570.1:c.*218T>G
|
ENSP00000493213.1:n.*218T>G
|
|
ENST00000641573.1:n.587T>G
|
|
|
ENST00000641587.1:c.*210T>G
|
ENSP00000493453.1:n.*210T>G
|
|
ENST00000641597.1:c.499T>G
|
ENSP00000493382.1:p.Phe167Val
|
|
ENST00000641756.1:c.*243T>G
|
ENSP00000493147.1:n.*243T>G
|
|
ENST00000641811.1:c.255T>G
|
|
|
ENST00000641847.1:n.358T>G
|
|
|
ENST00000641891.1:c.*325T>G
|
ENSP00000493288.1:n.*325T>G
|
|
ENST00000641927.1:n.439T>G
|
|
|
ENST00000641947.1:c.499T>G
|
ENSP00000492994.1:p.Phe167Val
|
|
ENST00000642021.1:n.621T>G
|
|
|
ENST00000369407.3:c.397T>G
|
ENSP00000358415.3:p.Phe133Val
|
|
ENST00000369409.8:c.499T>G
|
ENSP00000358417.4:p.Phe167Val
|
|
ENST00000462324.1:n.767T>G
|
|
|
ENST00000493622.5:n.688T>G
|
|
|
NM_006623.3:c.499T>G
|
NP_006614.2:p.Phe167Val
|
|
XM_011541226.1:c.721T>G
|
XP_011539528.1:p.Phe241Val
|
|
XM_011541227.1:c.643T>G
|
XP_011539529.1:p.Phe215Val
|
|
XM_011541228.1:c.610T>G
|
XP_011539530.1:p.Phe204Val
|
|
XM_011541229.1:c.436T>G
|
XP_011539531.1:p.Phe146Val
|
|
XM_011541230.1:c.214T>G
|
XP_011539532.1:p.Phe72Val
|
|
XM_011541231.1:c.205T>G
|
XP_011539533.1:p.Phe69Val
|
|
XM_011541226.2:c.721T>G
|
XP_011539528.1:p.Phe241Val
|
|
XM_011541227.2:c.643T>G
|
XP_011539529.1:p.Phe215Val
|
|
XM_011541228.2:c.610T>G
|
XP_011539530.1:p.Phe204Val
|
|
XM_011541231.2:c.205T>G
|
XP_011539533.1:p.Phe69Val
|
|
XM_024446338.1:c.610T>G
|
XP_024302106.1:p.Phe204Val
|
|
NM_006623.4:c.499T>G
MANE Select
|
NP_006614.2:p.Phe167Val
|
|