|
ENST00000700029.2:c.755A>C
|
ENSP00000514759.2:p.Asp252Ala
|
|
|
ENST00000710265.1:c.755A>C
|
ENSP00000518161.1:p.Asp252Ala
|
|
|
ENST00000472832.3:c.755A>C
|
ENSP00000483066.2:p.Asp252Ala
|
|
|
ENST00000688158.2:n.1490A>C
|
|
|
|
ENST00000688922.2:c.*585A>C
|
ENSP00000508742.2:n.*585A>C
|
|
|
ENST00000700021.1:c.710A>C
|
ENSP00000514757.1:p.Asp237Ala
|
|
|
ENST00000700022.1:c.*94A>C
|
ENSP00000514758.1:n.*94A>C
|
|
|
ENST00000700023.1:n.1913A>C
|
|
|
|
ENST00000700024.1:n.2147A>C
|
|
|
|
ENST00000700025.1:n.1524A>C
|
|
|
|
ENST00000700026.1:n.392A>C
|
|
|
|
ENST00000700029.1:c.589A>C
|
|
|
|
ENST00000706954.1:c.755A>C
|
ENSP00000516674.1:p.Asp252Ala
|
|
|
ENST00000706955.1:c.*790A>C
|
ENSP00000516675.1:n.*790A>C
|
|
|
ENST00000686459.1:c.*341A>C
|
ENSP00000508909.1:n.*341A>C
|
|
|
ENST00000688158.1:c.*866A>C
|
ENSP00000509254.1:n.*866A>C
|
|
|
ENST00000688308.1:c.755A>C
|
ENSP00000508752.1:p.Asp252Ala
|
|
|
ENST00000688922.1:c.676A>C
|
|
|
|
ENST00000693560.1:c.1274A>C
|
ENSP00000509861.1:p.Asp425Ala
|
|
|
ENST00000371953.8:c.755A>C
MANE Select
|
ENSP00000361021.3:p.Asp252Ala
|
|
|
ENST00000371953.7:c.755A>C
|
ENSP00000361021.3:p.Asp252Ala
|
|
|
ENST00000472832.2:c.182A>C
|
ENSP00000483066.1:p.Asp61Ala
|
|
|
NM_000314.5:c.755A>C
|
NP_000305.3:p.Asp252Ala
|
|
|
NM_000314.6:c.755A>C
|
NP_000305.3:p.Asp252Ala
|
|
|
NM_001304717.2:c.1274A>C
|
NP_001291646.2:p.Asp425Ala
|
|
|
NM_001304718.1:c.164A>C
|
NP_001291647.1:p.Asp55Ala
|
|
|
XM_006717926.2:c.710A>C
|
XP_006717989.1:p.Asp237Ala
|
|
|
XM_011539981.1:c.755A>C
|
XP_011538283.1:p.Asp252Ala
|
|
|
XM_011539982.1:c.659A>C
|
XP_011538284.1:p.Asp220Ala
|
|
|
XR_945791.1:n.1325A>C
|
|
|
|
NM_000314.7:c.755A>C
|
NP_000305.3:p.Asp252Ala
|
|
|
NM_001304717.5:c.1274A>C
|
NP_001291646.4:p.Asp425Ala
|
|
|
NM_001304718.2:c.164A>C
|
NP_001291647.1:p.Asp55Ala
|
|
|
NM_000314.8:c.755A>C
MANE Select
|
NP_000305.3:p.Asp252Ala
|
|
