ENST00000700228.1:c.1352A>T
|
ENSP00000514865.1:p.Lys451Met
|
|
ENST00000700229.1:c.520A>T
|
|
|
ENST00000700230.1:c.1096A>T
|
ENSP00000514867.1:n.1096A>T
|
|
ENST00000700231.1:c.1481A>T
|
ENSP00000514868.1:p.Lys494Met
|
|
ENST00000339562.9:c.1556A>T
MANE Select
|
ENSP00000344479.4:p.Lys519Met
|
|
ENST00000675870.1:c.*67A>T
|
ENSP00000502739.1:n.*67A>T
|
|
ENST00000339562.8:c.1556A>T
|
ENSP00000344479.4:p.Lys519Met
|
|
ENST00000409108.6:c.1452A>T
|
ENSP00000386993.2:p.Gln484His
|
|
ENST00000409572.5:c.1556A>T
|
ENSP00000386747.1:p.Lys519Met
|
|
ENST00000417764.5:c.*67A>T
|
ENSP00000415632.1:n.*67A>T
|
|
ENST00000417972.5:c.*67A>T
|
ENSP00000394671.1:n.*67A>T
|
|
ENST00000426264.5:c.1367A>T
|
ENSP00000389986.1:p.Lys456Met
|
|
ENST00000429376.5:c.1263A>T
|
ENSP00000410952.1:p.Gln421His
|
|
NM_006186.3:c.1556A>T
|
NP_006177.1:p.Lys519Met
|
|
XM_005246621.2:c.1589A>T
|
XP_005246678.1:p.Lys530Met
|
|
XM_005246622.2:c.1367A>T
|
XP_005246679.1:p.Lys456Met
|
|
XM_005246623.1:c.1367A>T
|
XP_005246680.1:p.Lys456Met
|
|
XM_006712553.2:c.1514A>T
|
XP_006712616.1:p.Lys505Met
|
|
XM_011511246.1:c.1485A>T
|
XP_011509548.1:p.Gln495His
|
|
XR_427087.2:n.3641A>T
|
|
|
NM_173173.2:c.1367A>T
|
NP_775265.1:p.Lys456Met
|
|
XM_005246621.4:c.1589A>T
|
XP_005246678.1:p.Lys530Met
|
|
XM_006712553.4:c.1514A>T
|
XP_006712616.1:p.Lys505Met
|
|
XM_011511246.2:c.1485A>T
|
XP_011509548.1:p.Gln495His
|
|
XM_017004219.2:c.1556A>T
|
XP_016859708.1:p.Lys519Met
|
|
XM_017004220.2:c.1481A>T
|
XP_016859709.1:p.Lys494Met
|
|
XR_001738751.2:n.1803A>T
|
|
|
XR_001738752.2:n.1625A>T
|
|
|
XR_427087.4:n.1682A>T
|
|
|
NM_006186.4:c.1556A>T
MANE Select
|
NP_006177.1:p.Lys519Met
|
|
NM_173173.3:c.1367A>T
|
NP_775265.1:p.Lys456Met
|
|