ENST00000391944.8:c.1981G>A
|
ENSP00000375808.4:p.Ala661Thr
|
|
ENST00000682414.1:c.1981G>A
|
ENSP00000507019.1:p.Ala661Thr
|
|
ENST00000682508.1:n.2010G>A
|
|
|
ENST00000684218.1:c.*1239G>A
|
ENSP00000507804.1:n.*1239G>A
|
|
ENST00000684264.1:n.1537G>A
|
|
|
ENST00000684407.1:c.1858G>A
|
ENSP00000507775.1:p.Ala620Thr
|
|
ENST00000684458.1:c.*467G>A
|
ENSP00000508260.1:n.*467G>A
|
|
ENST00000684468.1:n.1693G>A
|
|
|
ENST00000391945.10:c.1981G>A
MANE Select
|
ENSP00000375809.4:p.Ala661Thr
|
|
ENST00000646507.1:n.2078G>A
|
|
|
ENST00000391941.6:c.1909G>A
|
ENSP00000375805.2:p.Ala637Thr
|
|
ENST00000391942.6:n.1152G>A
|
|
|
ENST00000391944.7:c.1747G>A
|
ENSP00000375808.3:p.Ala583Thr
|
|
ENST00000391945.8:c.1981G>A
|
ENSP00000375809.3:p.Ala661Thr
|
|
ENST00000588652.5:n.2069G>A
|
|
|
NM_000400.3:c.1981G>A , LRG_461t1:c.1981G>A
|
NP_000391.1:p.Ala661Thr
|
|
XM_011526611.1:c.1903G>A
|
XP_011524913.1:p.Ala635Thr
|
|
XM_011526611.2:c.1903G>A
|
XP_011524913.1:p.Ala635Thr
|
|
XM_017026467.1:c.1858G>A
|
XP_016881956.1:p.Ala620Thr
|
|
XR_001753633.2:n.2028G>A
|
|
|
XR_001753634.2:n.1964G>A
|
|
|
NM_000400.4:c.1981G>A
MANE Select
|
NP_000391.1:p.Ala661Thr
|
|