|
ENST00000494804.2:n.2427G>A
|
|
|
|
ENST00000517337.2:c.879G>A
|
ENSP00000429971.2:p.Trp293Ter
|
|
|
ENST00000523444.2:c.879G>A
|
ENSP00000428252.2:p.Trp293Ter
|
|
|
ENST00000697292.1:c.1125G>A
|
ENSP00000513229.1:p.Trp375Ter
|
|
|
ENST00000697293.1:c.1125G>A
|
ENSP00000513230.1:p.Trp375Ter
|
|
|
ENST00000697294.1:c.*736G>A
|
ENSP00000513231.1:n.*736G>A
|
|
|
ENST00000697295.1:c.*434G>A
|
ENSP00000513232.1:n.*434G>A
|
|
|
ENST00000697296.1:c.*793G>A
|
ENSP00000513233.1:n.*793G>A
|
|
|
ENST00000697297.1:n.2910G>A
|
|
|
|
ENST00000697298.1:c.879G>A
|
ENSP00000513234.1:p.Trp293Ter
|
|
|
ENST00000697299.1:c.879G>A
|
ENSP00000513235.1:p.Trp293Ter
|
|
|
ENST00000697300.1:c.*729G>A
|
ENSP00000513236.1:n.*729G>A
|
|
|
ENST00000697301.1:c.*646G>A
|
ENSP00000513237.1:n.*646G>A
|
|
|
ENST00000697302.1:c.*646G>A
|
ENSP00000513238.1:n.*646G>A
|
|
|
ENST00000697303.1:c.*729G>A
|
ENSP00000513239.1:n.*729G>A
|
|
|
ENST00000697304.1:c.813G>A
|
ENSP00000513240.1:p.Trp271Ter
|
|
|
ENST00000697306.1:c.*125G>A
|
ENSP00000513241.1:n.*125G>A
|
|
|
ENST00000697307.1:c.1125G>A
|
ENSP00000513242.1:p.Trp375Ter
|
|
|
ENST00000697308.1:c.1125G>A
|
ENSP00000513243.1:p.Trp375Ter
|
|
|
ENST00000697309.1:c.1125G>A
|
ENSP00000513244.1:p.Trp375Ter
|
|
|
ENST00000697310.1:c.1125G>A
|
ENSP00000513245.1:p.Trp375Ter
|
|
|
ENST00000697311.1:c.1125G>A
|
ENSP00000513246.1:p.Trp375Ter
|
|
|
ENST00000697312.1:c.*523G>A
|
ENSP00000513247.1:n.*523G>A
|
|
|
ENST00000697313.1:n.2687+14809G>A
|
|
|
|
ENST00000697314.1:n.2916G>A
|
|
|
|
ENST00000697315.1:c.1125G>A
|
ENSP00000513248.1:p.Trp375Ter
|
|
|
ENST00000697316.1:n.1246G>A
|
|
|
|
ENST00000697317.1:n.1235G>A
|
|
|
|
ENST00000697318.1:n.1237G>A
|
|
|
|
ENST00000265433.8:c.1125G>A
MANE Select
|
ENSP00000265433.4:p.Trp375Ter
|
|
|
ENST00000265433.7:c.1125G>A
|
ENSP00000265433.3:p.Trp375Ter
|
|
|
ENST00000396252.6:c.*998G>A
|
ENSP00000379551.2:n.*998G>A
|
|
|
ENST00000409330.5:c.879G>A
|
ENSP00000386924.1:p.Trp293Ter
|
|
|
NM_001024688.2:c.879G>A
|
NP_001019859.1:p.Trp293Ter
|
|
|
NM_002485.4:c.1125G>A , LRG_158t1:c.1125G>A
|
NP_002476.2:p.Trp375Ter
|
|
|
XM_011517044.1:c.1101G>A
|
XP_011515346.1:p.Trp367Ter
|
|
|
XM_011517045.1:c.879G>A
|
XP_011515347.1:p.Trp293Ter
|
|
|
XM_011517046.1:c.1125G>A
|
XP_011515348.1:p.Trp375Ter
|
|
|
XR_928335.1:n.1262G>A
|
|
|
|
XM_017013460.1:c.246G>A
|
XP_016868949.1:p.Trp82Ter
|
|
|
XM_017013462.2:c.246G>A
|
XP_016868951.1:p.Trp82Ter
|
|
|
XM_024447163.1:c.879G>A
|
XP_024302931.1:p.Trp293Ter
|
|
|
XM_024447164.1:c.879G>A
|
XP_024302932.1:p.Trp293Ter
|
|
|
XM_024447165.1:c.246G>A
|
XP_024302933.1:p.Trp82Ter
|
|
|
NM_002485.5:c.1125G>A
MANE Select
|
NP_002476.2:p.Trp375Ter
|
|
|
NM_001024688.3:c.879G>A
|
NP_001019859.1:p.Trp293Ter
|
|
