|
ENST00000361510.8:c.2088G>A
MANE Select
|
ENSP00000355324.2:p.Ala696=
|
|
|
ENST00000361828.7:c.1923G>A
|
ENSP00000354429.3:p.Ala641=
|
|
|
ENST00000361908.8:c.2034G>A
|
ENSP00000354681.3:p.Ala678=
|
|
|
ENST00000392436.7:c.1923G>A
|
ENSP00000376231.3:p.Ala641=
|
|
|
ENST00000392437.6:c.1977G>A
|
ENSP00000376232.2:p.Ala659=
|
|
|
ENST00000642289.1:c.1862G>A
|
|
|
|
ENST00000642445.1:c.1923G>A
|
ENSP00000495535.1:p.Ala641=
|
|
|
ENST00000642593.1:c.*148G>A
|
ENSP00000494273.1:n.*148G>A
|
|
|
ENST00000643329.1:c.1605G>A
|
ENSP00000493673.1:p.Ala535=
|
|
|
ENST00000643737.1:c.*2004G>A
|
ENSP00000494210.1:n.*2004G>A
|
|
|
ENST00000644595.1:c.1923G>A
|
ENSP00000494121.1:p.Ala641=
|
|
|
ENST00000644629.1:c.1510G>A
|
|
|
|
ENST00000644841.1:c.*407G>A
|
ENSP00000493988.1:n.*407G>A
|
|
|
ENST00000644959.1:c.1892G>A
|
|
|
|
ENST00000645553.1:c.1938G>A
|
ENSP00000494725.1:p.Ala646=
|
|
|
ENST00000646085.1:c.*1401G>A
|
ENSP00000494509.1:n.*1401G>A
|
|
|
ENST00000646277.1:c.*524G>A
|
ENSP00000495289.1:n.*524G>A
|
|
|
ENST00000646544.1:c.911G>A
|
|
|
|
ENST00000646699.1:c.1862G>A
|
|
|
|
ENST00000646793.1:c.1815G>A
|
ENSP00000494512.1:p.Ala605=
|
|
|
ENST00000361150.6:c.1926G>A
|
ENSP00000354781.2:p.Ala642=
|
|
|
ENST00000361510.6:c.2088G>A
|
ENSP00000355324.2:p.Ala696=
|
|
|
ENST00000361715.6:c.1980G>A
|
ENSP00000355311.2:p.Ala660=
|
|
|
ENST00000361828.6:c.1977G>A
|
ENSP00000354429.2:p.Ala659=
|
|
|
ENST00000361908.7:c.2034G>A
|
ENSP00000354681.3:p.Ala678=
|
|
|
ENST00000392438.7:c.1923G>A
|
ENSP00000376233.3:p.Ala641=
|
|
|
ENST00000482865.1:n.182G>A
|
|
|
|
NM_015560.2:c.1923G>A , LRG_337t1:c.1923G>A
|
NP_056375.2:p.Ala641=
|
|
|
NM_130831.2:c.1815G>A
|
NP_570844.1:p.Ala605=
|
|
|
NM_130832.2:c.1869G>A
|
NP_570845.1:p.Ala623=
|
|
|
NM_130833.2:c.1926G>A
|
NP_570846.1:p.Ala642=
|
|
|
NM_130834.2:c.1977G>A
|
NP_570847.2:p.Ala659=
|
|
|
NM_130835.2:c.1980G>A
|
NP_570848.1:p.Ala660=
|
|
|
NM_130836.2:c.2034G>A
|
NP_570849.2:p.Ala678=
|
|
|
NM_130837.2:c.2088G>A , LRG_337t2:c.2088G>A
|
NP_570850.2:p.Ala696=
|
|
|
XM_011512863.1:c.2088G>A
|
XP_011511165.1:p.Ala696=
|
|
|
XM_011512864.1:c.2034G>A
|
XP_011511166.1:p.Ala678=
|
|
|
XM_011512865.1:c.1977G>A
|
XP_011511167.1:p.Ala659=
|
|
|
XM_011512866.1:c.1926G>A
|
XP_011511168.1:p.Ala642=
|
|
|
XM_011512867.1:c.1923G>A
|
XP_011511169.1:p.Ala641=
|
|
|
XM_011512868.1:c.1815G>A
|
XP_011511170.1:p.Ala605=
|
|
|
XM_011512869.1:c.2088G>A
|
XP_011511171.1:p.Ala696=
|
|
|
XR_924835.1:n.583-7627C>T
|
|
|
|
NM_001354663.1:c.1554G>A
|
NP_001341592.1:p.Ala518=
|
|
|
NM_001354664.1:c.1551G>A
|
NP_001341593.1:p.Ala517=
|
|
|
XR_001740158.2:n.2317G>A
|
|
|
|
XR_001740159.2:n.2152G>A
|
|
|
|
XR_001741074.1:n.476-7627C>T
|
|
|
|
XR_924835.2:n.601-7627C>T
|
|
|
|
NM_001354663.2:c.1554G>A
|
NP_001341592.1:p.Ala518=
|
|
|
NM_001354664.2:c.1551G>A
|
NP_001341593.1:p.Ala517=
|
|
|
NM_130831.3:c.1815G>A
|
NP_570844.1:p.Ala605=
|
|
|
NM_130832.3:c.1869G>A
|
NP_570845.1:p.Ala623=
|
|
|
NM_130834.3:c.1977G>A
|
NP_570847.2:p.Ala659=
|
|
|
NM_130836.3:c.2034G>A
|
NP_570849.2:p.Ala678=
|
|
|
NM_015560.3:c.1923G>A
|
NP_056375.2:p.Ala641=
|
|
|
NM_130833.3:c.1926G>A
|
NP_570846.1:p.Ala642=
|
|
|
NM_130835.3:c.1980G>A
|
NP_570848.1:p.Ala660=
|
|
|
NM_130837.3:c.2088G>A
MANE Select
|
NP_570850.2:p.Ala696=
|
|
