|
ENST00000340913.11:c.999T>G
MANE Select
|
ENSP00000341826.7:p.Phe333Leu
|
|
|
ENST00000550482.2:c.843T>G
|
ENSP00000446486.2:p.Phe281Leu
|
|
|
ENST00000676472.1:c.131T>G
|
|
|
|
ENST00000676572.1:c.225T>G
|
|
|
|
ENST00000676707.1:c.146T>G
|
|
|
|
ENST00000676725.1:n.1173T>G
|
|
|
|
ENST00000676794.1:c.18T>G
|
ENSP00000504819.1:p.Phe6Leu
|
|
|
ENST00000676853.1:c.227T>G
|
|
|
|
ENST00000676886.1:c.85-355T>G
|
|
|
|
ENST00000676951.1:c.248T>G
|
|
|
|
ENST00000677191.1:c.339T>G
|
|
|
|
ENST00000677210.1:c.999T>G
|
ENSP00000503610.1:p.Phe333Leu
|
|
|
ENST00000677220.1:c.132+2401T>G
|
ENSP00000502987.1:n.132+2401T>G
|
|
|
ENST00000677224.1:c.101T>G
|
|
|
|
ENST00000677249.1:c.840T>G
|
ENSP00000503649.1:p.Phe280Leu
|
|
|
ENST00000677279.1:c.98T>G
|
|
|
|
ENST00000677375.1:c.843T>G
|
ENSP00000503651.1:p.Phe281Leu
|
|
|
ENST00000677385.1:c.*1185T>G
|
ENSP00000502985.1:n.*1185T>G
|
|
|
ENST00000677518.1:c.92T>G
|
|
|
|
ENST00000677539.1:c.381T>G
|
|
|
|
ENST00000677636.1:c.185T>G
|
|
|
|
ENST00000677778.1:c.75+1029T>G
|
|
|
|
ENST00000677840.1:c.92T>G
|
|
|
|
ENST00000677847.1:c.32T>G
|
|
|
|
ENST00000677945.1:c.170T>G
|
|
|
|
ENST00000678077.1:c.708T>G
|
ENSP00000504814.1:p.Phe236Leu
|
|
|
ENST00000678212.1:c.187T>G
|
|
|
|
ENST00000678279.1:n.78T>G
|
|
|
|
ENST00000678365.1:n.49-2759T>G
|
|
|
|
ENST00000678412.1:c.157-355T>G
|
|
|
|
ENST00000678418.1:n.1195T>G
|
|
|
|
ENST00000678424.1:c.224T>G
|
|
|
|
ENST00000678448.1:c.191T>G
|
ENSP00000503619.1:n.191T>G
|
|
|
ENST00000678456.1:c.76-355T>G
|
|
|
|
ENST00000678513.1:c.119T>G
|
|
|
|
ENST00000678581.1:c.227T>G
|
|
|
|
ENST00000678597.1:c.116T>G
|
|
|
|
ENST00000678611.1:c.233T>G
|
|
|
|
ENST00000678873.1:c.167T>G
|
|
|
|
ENST00000678876.1:c.185T>G
|
|
|
|
ENST00000678934.1:c.146T>G
|
|
|
|
ENST00000678970.1:c.168T>G
|
|
|
|
ENST00000679026.1:c.92T>G
|
|
|
|
ENST00000679063.1:c.167T>G
|
|
|
|
ENST00000679079.1:c.157-646T>G
|
|
|
|
ENST00000679228.1:n.1194T>G
|
|
|
|
ENST00000679273.1:c.179T>G
|
ENSP00000504626.1:n.179T>G
|
|
|
ENST00000679344.1:c.200T>G
|
|
|
|
ENST00000330752.12:c.804T>G
|
ENSP00000333504.8:p.Phe268Leu
|
|
|
ENST00000340913.10:c.999T>G
|
ENSP00000341826.6:p.Phe333Leu
|
|
|
ENST00000546500.5:c.843T>G
|
ENSP00000448617.1:p.Phe281Leu
|
|
|
ENST00000547276.5:c.684T>G
|
ENSP00000447260.1:p.Phe228Leu
|
|
|
ENST00000547566.5:c.843T>G
|
ENSP00000449913.1:p.Phe281Leu
|
|
|
ENST00000550482.1:c.456T>G
|
ENSP00000446486.1:p.Phe152Leu
|
|
|
ENST00000551679.1:n.181T>G
|
|
|
|
NM_002136.2:c.843T>G
|
NP_002127.1:p.Phe281Leu
|
|
|
NM_031157.2:c.999T>G
|
NP_112420.1:p.Phe333Leu
|
|
|
XM_005268826.1:c.999T>G
|
XP_005268883.1:p.Phe333Leu
|
|
|
XR_245923.1:n.1111T>G
|
|
|
|
XR_245924.1:n.955T>G
|
|
|
|
NM_002136.3:c.843T>G
|
NP_002127.1:p.Phe281Leu
|
|
|
NM_031157.3:c.999T>G
|
NP_112420.1:p.Phe333Leu
|
|
|
NR_135167.1:n.961T>G
|
|
|
|
XM_005268826.2:c.999T>G
|
XP_005268883.1:p.Phe333Leu
|
|
|
XR_245923.2:n.1071T>G
|
|
|
|
NM_002136.4:c.843T>G
|
NP_002127.1:p.Phe281Leu
|
|
|
NM_031157.4:c.999T>G
MANE Select
|
NP_112420.1:p.Phe333Leu
|
|
|
NR_135167.2:n.925T>G
|
|
|
