ENST00000620350.5:c.*49G>T
MANE Select
|
ENSP00000484634.1:n.*49G>T
|
|
ENST00000250173.5:c.*314G>T
|
ENSP00000250173.2:n.*314G>T
|
|
ENST00000518642.5:c.*314G>T
|
ENSP00000428610.1:n.*314G>T
|
|
ENST00000519595.5:c.*49G>T
|
ENSP00000429791.1:n.*49G>T
|
|
ENST00000522789.5:c.670G>T
|
ENSP00000428015.1:n.670G>T
|
|
ENST00000618342.1:c.1450G>T
|
ENSP00000484802.1:n.1450G>T
|
|
ENST00000620350.4:c.*49G>T
|
ENSP00000484634.1:n.*49G>T
|
|
NM_012472.4:c.*49G>T
|
NP_036604.2:n.*49G>T
|
|
NR_073525.1:n.1674G>T
|
|
|
XM_006716538.2:c.*49G>T
|
XP_006716601.2:n.*49G>T
|
|
XM_011516950.1:c.*49G>T
|
XP_011515252.1:n.*49G>T
|
|
XM_011516952.1:c.*49G>T
|
XP_011515254.1:n.*49G>T
|
|
XM_011516953.1:c.*49G>T
|
XP_011515255.1:n.*49G>T
|
|
XM_011516954.1:c.*49G>T
|
XP_011515256.1:n.*49G>T
|
|
XR_428377.2:n.1702G>T
|
|
|
NM_001321961.1:c.*49G>T
|
NP_001308890.1:n.*49G>T
|
|
NM_001321962.1:c.*49G>T
|
NP_001308891.1:n.*49G>T
|
|
NM_001321963.1:c.*49G>T
|
NP_001308892.1:n.*49G>T
|
|
NM_001321964.1:c.*49G>T
|
NP_001308893.1:n.*49G>T
|
|
NM_001321965.1:c.*49G>T
|
NP_001308894.1:n.*49G>T
|
|
NM_001321966.1:c.*49G>T
|
NP_001308895.1:n.*49G>T
|
|
NM_012472.5:c.*49G>T
|
NP_036604.2:n.*49G>T
|
|
NR_073525.2:n.1674G>T
|
|
|
NR_135905.1:n.1663G>T
|
|
|
NR_135906.1:n.1104G>T
|
|
|
NR_135907.1:n.1350G>T
|
|
|
NR_135908.1:n.1044G>T
|
|
|
NR_135909.1:n.1468G>T
|
|
|
NR_135910.1:n.1775G>T
|
|
|
NR_135911.1:n.1854G>T
|
|
|
NR_135912.1:n.2413G>T
|
|
|
NR_135913.1:n.2100G>T
|
|
|
XM_006716538.3:c.*49G>T
|
XP_006716601.2:n.*49G>T
|
|
XM_011516950.2:c.*49G>T
|
XP_011515252.1:n.*49G>T
|
|
XM_017013296.1:c.*49G>T
|
XP_016868785.1:n.*49G>T
|
|
XM_017013297.1:c.*49G>T
|
XP_016868786.1:n.*49G>T
|
|
XM_017013298.1:c.*49G>T
|
XP_016868787.1:n.*49G>T
|
|
NM_012472.6:c.*49G>T
MANE Select
|
NP_036604.2:n.*49G>T
|
|
NM_001321961.2:c.*49G>T
|
NP_001308890.1:n.*49G>T
|
|
NM_001321962.2:c.*49G>T
|
NP_001308891.1:n.*49G>T
|
|
NM_001321963.2:c.*49G>T
|
NP_001308892.1:n.*49G>T
|
|
NM_001321964.2:c.*49G>T
|
NP_001308893.1:n.*49G>T
|
|
NM_001321965.2:c.*49G>T
|
NP_001308894.1:n.*49G>T
|
|
NM_001321966.2:c.*49G>T
|
NP_001308895.1:n.*49G>T
|
|
NR_073525.3:n.1602G>T
|
|
|
NR_135905.2:n.1591G>T
|
|
|
NR_135906.2:n.1032G>T
|
|
|
NR_135907.2:n.1278G>T
|
|
|
NR_135908.2:n.972G>T
|
|
|
NR_135909.2:n.1488G>T
|
|
|
NR_135910.2:n.1838G>T
|
|
|
NR_135911.2:n.1958G>T
|
|
|
NR_135912.2:n.2517G>T
|
|
|
NR_135913.2:n.2204G>T
|
|
|