ENST00000646519.1:c.*650G>C
|
ENSP00000496517.1:n.*650G>C
|
|
ENST00000647337.2:c.1493G>C
MANE Select
|
ENSP00000495497.1:p.Gly498Ala
|
|
ENST00000359524.7:c.1451G>C
|
ENSP00000352514.5:p.Gly484Ala
|
|
ENST00000371432.7:c.1427G>C
|
ENSP00000360486.4:p.Gly476Ala
|
|
ENST00000371436.10:c.1427G>C
|
ENSP00000360491.6:p.Gly476Ala
|
|
ENST00000371438.5:c.1493G>C
|
ENSP00000360493.1:p.Gly498Ala
|
|
ENST00000465038.6:c.1493G>C
|
ENSP00000420707.2:p.Gly498Ala
|
|
ENST00000478660.6:c.*178+33579G>C
|
ENSP00000460188.1:n.*178+33579G>C
|
|
ENST00000576263.5:c.1021+34825G>C
|
ENSP00000458178.1:n.1021+34825G>C
|
|
ENST00000625924.1:c.1385G>C
|
ENSP00000485863.1:p.Gly462Ala
|
|
NM_001015051.3:c.1427G>C
|
NP_001015051.3:p.Gly476Ala
|
|
NM_001024630.3:c.1493G>C
|
NP_001019801.3:p.Gly498Ala
|
|
NM_001278478.1:c.1385G>C
|
NP_001265407.1:p.Gly462Ala
|
|
XM_006715232.1:c.1277G>C
|
XP_006715295.1:p.Gly426Ala
|
|
XM_011514960.1:c.1225+34825G>C
|
XP_011513262.1:n.1225+34825G>C
|
|
XM_011514961.1:c.1697G>C
|
XP_011513263.1:p.Gly566Ala
|
|
XM_011514962.1:c.1631G>C
|
XP_011513264.1:p.Gly544Ala
|
|
XM_011514963.1:c.1051+34825G>C
|
XP_011513265.1:n.1051+34825G>C
|
|
XM_011514964.1:c.1435+262G>C
|
XP_011513266.1:n.1435+262G>C
|
|
XM_011514966.1:c.553+34825G>C
|
XP_011513268.1:n.553+34825G>C
|
|
NM_001024630.4:c.1493G>C
MANE Select
|
NP_001019801.3:p.Gly498Ala
|
|
NM_001278478.2:c.1385G>C
|
NP_001265407.1:p.Gly462Ala
|
|
NM_001369405.1:c.1451G>C
|
NP_001356334.1:p.Gly484Ala
|
|
NM_001015051.4:c.1427G>C
|
NP_001015051.3:p.Gly476Ala
|
|