ENST00000646519.1:c.*954T>C
|
ENSP00000496517.1:n.*954T>C
|
|
ENST00000647337.2:c.*231T>C
MANE Select
|
ENSP00000495497.1:n.*231T>C
|
|
ENST00000359524.7:c.*231T>C
|
ENSP00000352514.5:n.*231T>C
|
|
ENST00000371432.7:c.*231T>C
|
ENSP00000360486.4:n.*231T>C
|
|
ENST00000371438.5:c.*231T>C
|
ENSP00000360493.1:n.*231T>C
|
|
ENST00000478660.6:c.*178+33883T>C
|
ENSP00000460188.1:n.*178+33883T>C
|
|
ENST00000576263.5:c.1021+35129T>C
|
ENSP00000458178.1:n.1021+35129T>C
|
|
NM_001015051.3:c.*231T>C
|
NP_001015051.3:n.*231T>C
|
|
NM_001024630.3:c.*231T>C
|
NP_001019801.3:n.*231T>C
|
|
NM_001278478.1:c.1689T>C
|
NP_001265407.1:n.1689T>C
|
|
XM_006715232.1:c.*231T>C
|
XP_006715295.1:n.*231T>C
|
|
XM_011514960.1:c.1225+35129T>C
|
XP_011513262.1:n.1225+35129T>C
|
|
XM_011514961.1:c.*231T>C
|
XP_011513263.1:n.*231T>C
|
|
XM_011514962.1:c.*231T>C
|
XP_011513264.1:n.*231T>C
|
|
XM_011514963.1:c.1051+35129T>C
|
XP_011513265.1:n.1051+35129T>C
|
|
XM_011514964.1:c.1435+566T>C
|
XP_011513266.1:n.1435+566T>C
|
|
XM_011514966.1:c.553+35129T>C
|
XP_011513268.1:n.553+35129T>C
|
|
NM_001024630.4:c.*231T>C
MANE Select
|
NP_001019801.3:n.*231T>C
|
|
NM_001278478.2:c.*231T>C
|
NP_001265407.1:n.*231T>C
|
|
NM_001369405.1:c.*231T>C
|
NP_001356334.1:n.*231T>C
|
|
NM_001015051.4:c.*231T>C
|
NP_001015051.3:n.*231T>C
|
|