ENST00000371418.9:c.676T>G
MANE Select
|
ENSP00000360472.4:p.Phe226Val
|
|
ENST00000485458.3:n.4652T>G
|
|
|
ENST00000635953.1:c.676T>G
|
ENSP00000490058.1:p.Phe226Val
|
|
ENST00000636155.1:c.676T>G
|
ENSP00000490355.1:p.Phe226Val
|
|
ENST00000636232.1:c.*462T>G
|
ENSP00000490325.1:n.*462T>G
|
|
ENST00000636754.1:c.*518T>G
|
ENSP00000489781.1:n.*518T>G
|
|
ENST00000636946.1:c.*845T>G
|
ENSP00000490654.1:n.*845T>G
|
|
ENST00000637037.1:c.*266T>G
|
ENSP00000490860.1:n.*266T>G
|
|
ENST00000637347.1:n.537T>G
|
|
|
ENST00000637611.1:c.*232T>G
|
ENSP00000489682.1:n.*232T>G
|
|
ENST00000637689.1:c.-696T>G
|
ENSP00000490496.1:n.-696T>G
|
|
ENST00000637925.1:c.*271T>G
|
ENSP00000489763.1:n.*271T>G
|
|
ENST00000638049.1:c.*434T>G
|
ENSP00000490597.1:n.*434T>G
|
|
ENST00000676175.1:n.2415T>G
|
|
|
ENST00000371413.4:c.676T>G
|
ENSP00000360467.3:p.Phe226Val
|
|
ENST00000371418.8:c.676T>G
|
ENSP00000360472.4:p.Phe226Val
|
|
ENST00000626307.1:n.4591T>G
|
|
|
ENST00000626946.1:n.346T>G
|
|
|
ENST00000627420.2:c.*385T>G
|
ENSP00000487116.1:n.*385T>G
|
|
ENST00000629035.2:c.604T>G
|
ENSP00000486908.1:p.Phe202Val
|
|
ENST00000630047.2:c.532T>G
|
ENSP00000485917.1:p.Phe178Val
|
|
ENST00000630412.1:n.464T>G
|
|
|
ENST00000630487.2:c.*466T>G
|
ENSP00000486859.1:n.*466T>G
|
|
NM_001308275.1:c.676T>G
|
NP_001295204.1:p.Phe226Val
|
|
NM_001308276.1:c.532T>G
|
NP_001295205.1:p.Phe178Val
|
|
NM_005097.2:c.676T>G
|
NP_005088.1:p.Phe226Val
|
|
NM_005097.3:c.676T>G
|
NP_005088.1:p.Phe226Val
|
|
NR_131777.1:n.940T>G
|
|
|
XM_017016911.2:c.676T>G
|
XP_016872400.1:p.Phe226Val
|
|
XM_017016912.2:c.532T>G
|
XP_016872401.1:p.Phe178Val
|
|
NM_005097.4:c.676T>G
MANE Select
|
NP_005088.1:p.Phe226Val
|
|
NM_001308275.2:c.676T>G
|
NP_001295204.1:p.Phe226Val
|
|
NM_001308276.2:c.532T>G
|
NP_001295205.1:p.Phe178Val
|
|
NR_131777.2:n.813T>G
|
|
|