ENST00000584322.2:c.2363A>C
|
ENSP00000463272.2:p.Asn788Thr
|
|
ENST00000682066.1:c.2493A>C
|
ENSP00000507191.1:n.2493A>C
|
|
ENST00000682073.1:n.1103A>C
|
|
|
ENST00000682433.1:n.1442A>C
|
|
|
ENST00000682453.1:c.2363A>C
|
ENSP00000506943.1:p.Asn788Thr
|
|
ENST00000682477.1:c.*1789A>C
|
ENSP00000507075.1:n.*1789A>C
|
|
ENST00000682589.1:n.8240A>C
|
|
|
ENST00000682755.1:c.2141A>C
|
ENSP00000507660.1:p.Asn714Thr
|
|
ENST00000682989.1:c.2363A>C
|
ENSP00000507786.1:p.Asn788Thr
|
|
ENST00000683039.1:c.2363A>C
|
ENSP00000508303.1:p.Asn788Thr
|
|
ENST00000683235.1:c.2363A>C
|
ENSP00000507646.1:p.Asn788Thr
|
|
ENST00000683381.1:c.2423A>C
|
ENSP00000508184.1:p.Asn808Thr
|
|
ENST00000683535.1:n.493A>C
|
|
|
ENST00000684471.1:n.776A>C
|
|
|
ENST00000684584.1:c.1856A>C
|
ENSP00000508044.1:p.Asn619Thr
|
|
ENST00000684769.1:c.428A>C
|
ENSP00000507691.1:p.Asn143Thr
|
|
ENST00000259008.7:c.2363A>C
MANE Select
|
ENSP00000259008.2:p.Asn788Thr
|
|
ENST00000259008.6:c.2363A>C
|
ENSP00000259008.2:p.Asn788Thr
|
|
ENST00000577598.5:c.2363A>C
|
ENSP00000464654.1:p.Asn788Thr
|
|
ENST00000584322.1:c.346A>C
|
|
|
NM_032043.2:c.2363A>C , LRG_300t1:c.2363A>C
|
NP_114432.2:p.Asn788Thr
|
|
XM_011525332.1:c.2423A>C
|
XP_011523634.1:p.Asn808Thr
|
|
XM_011525333.1:c.2423A>C
|
XP_011523635.1:p.Asn808Thr
|
|
XM_011525334.1:c.2423A>C
|
XP_011523636.1:p.Asn808Thr
|
|
XM_011525335.1:c.2363A>C
|
XP_011523637.1:p.Asn788Thr
|
|
XM_011525336.1:c.2303A>C
|
XP_011523638.1:p.Asn768Thr
|
|
XM_011525337.1:c.2222A>C
|
XP_011523639.1:p.Asn741Thr
|
|
XM_011525338.1:c.1940A>C
|
XP_011523640.1:p.Asn647Thr
|
|
XM_011525339.1:c.2423A>C
|
XP_011523641.1:p.Asn808Thr
|
|
XM_011525340.1:c.2423A>C
|
XP_011523642.1:p.Asn808Thr
|
|
XR_934894.1:n.524-1152T>G
|
|
|
XM_011525332.3:c.2423A>C
|
XP_011523634.1:p.Asn808Thr
|
|
XM_011525333.3:c.2423A>C
|
XP_011523635.1:p.Asn808Thr
|
|
XM_011525334.2:c.2423A>C
|
XP_011523636.1:p.Asn808Thr
|
|
XM_011525335.3:c.2363A>C
|
XP_011523637.1:p.Asn788Thr
|
|
XM_011525336.2:c.2303A>C
|
XP_011523638.1:p.Asn768Thr
|
|
XM_011525337.2:c.2222A>C
|
XP_011523639.1:p.Asn741Thr
|
|
XM_011525338.2:c.1940A>C
|
XP_011523640.1:p.Asn647Thr
|
|
XM_011525339.3:c.2423A>C
|
XP_011523641.1:p.Asn808Thr
|
|
XM_011525340.3:c.2423A>C
|
XP_011523642.1:p.Asn808Thr
|
|
XM_017025200.1:c.1880A>C
|
XP_016880689.1:p.Asn627Thr
|
|
XM_017025201.1:c.1880A>C
|
XP_016880690.1:p.Asn627Thr
|
|
XM_017025202.1:c.509A>C
|
XP_016880691.1:p.Asn170Thr
|
|
XM_017025203.1:c.509A>C
|
XP_016880692.1:p.Asn170Thr
|
|
NM_032043.3:c.2363A>C
MANE Select
|
NP_114432.2:p.Asn788Thr
|
|