|
ENST00000700029.2:c.904T>G
|
ENSP00000514759.2:p.Phe302Val
|
|
|
ENST00000710265.1:c.811T>G
|
ENSP00000518161.1:p.Phe271Val
|
|
|
ENST00000472832.3:c.811T>G
|
ENSP00000483066.2:p.Phe271Val
|
|
|
ENST00000688158.2:n.1546T>G
|
|
|
|
ENST00000688922.2:c.*641T>G
|
ENSP00000508742.2:n.*641T>G
|
|
|
ENST00000700021.1:c.766T>G
|
ENSP00000514757.1:p.Phe256Val
|
|
|
ENST00000700022.1:c.*150T>G
|
ENSP00000514758.1:n.*150T>G
|
|
|
ENST00000700023.1:n.1969T>G
|
|
|
|
ENST00000700024.1:n.2203T>G
|
|
|
|
ENST00000700025.1:n.1580T>G
|
|
|
|
ENST00000700026.1:n.448T>G
|
|
|
|
ENST00000700029.1:c.738T>G
|
|
|
|
ENST00000706954.1:c.811T>G
|
ENSP00000516674.1:p.Phe271Val
|
|
|
ENST00000706955.1:c.*846T>G
|
ENSP00000516675.1:n.*846T>G
|
|
|
ENST00000686459.1:c.*397T>G
|
ENSP00000508909.1:n.*397T>G
|
|
|
ENST00000688158.1:c.*922T>G
|
ENSP00000509254.1:n.*922T>G
|
|
|
ENST00000688308.1:c.811T>G
|
ENSP00000508752.1:p.Phe271Val
|
|
|
ENST00000688922.1:c.732T>G
|
|
|
|
ENST00000693560.1:c.1330T>G
|
ENSP00000509861.1:p.Phe444Val
|
|
|
ENST00000371953.8:c.811T>G
MANE Select
|
ENSP00000361021.3:p.Phe271Val
|
|
|
ENST00000371953.7:c.811T>G
|
ENSP00000361021.3:p.Phe271Val
|
|
|
ENST00000472832.2:c.238T>G
|
ENSP00000483066.1:p.Phe80Val
|
|
|
NM_000314.5:c.811T>G
|
NP_000305.3:p.Phe271Val
|
|
|
NM_000314.6:c.811T>G
|
NP_000305.3:p.Phe271Val
|
|
|
NM_001304717.2:c.1330T>G
|
NP_001291646.2:p.Phe444Val
|
|
|
NM_001304718.1:c.220T>G
|
NP_001291647.1:p.Phe74Val
|
|
|
XM_006717926.2:c.766T>G
|
XP_006717989.1:p.Phe256Val
|
|
|
XM_011539981.1:c.811T>G
|
XP_011538283.1:p.Phe271Val
|
|
|
XM_011539982.1:c.715T>G
|
XP_011538284.1:p.Phe239Val
|
|
|
XR_945791.1:n.1381T>G
|
|
|
|
NM_000314.7:c.811T>G
|
NP_000305.3:p.Phe271Val
|
|
|
NM_001304717.5:c.1330T>G
|
NP_001291646.4:p.Phe444Val
|
|
|
NM_001304718.2:c.220T>G
|
NP_001291647.1:p.Phe74Val
|
|
|
NM_000314.8:c.811T>G
MANE Select
|
NP_000305.3:p.Phe271Val
|
|
