ENST00000304874.14:c.1345G>T
MANE Select
|
ENSP00000307188.9:p.Asp449Tyr
|
|
ENST00000362000.10:c.1150G>T
|
ENSP00000354710.6:p.Asp384Tyr
|
|
ENST00000380839.9:c.1267G>T
|
ENSP00000370219.4:p.Asp423Tyr
|
|
ENST00000395331.4:c.1285G>T
|
ENSP00000378740.3:p.Asp429Tyr
|
|
ENST00000395332.8:c.1345G>T
|
ENSP00000378741.3:p.Asp449Tyr
|
|
ENST00000488343.2:c.148-42G>T
|
ENSP00000500864.1:n.148-42G>T
|
|
ENST00000672498.1:c.*748G>T
|
ENSP00000500227.1:n.*748G>T
|
|
ENST00000672586.1:n.2104G>T
|
|
|
ENST00000672676.1:n.2369G>T
|
|
|
ENST00000673149.1:n.1157G>T
|
|
|
ENST00000673350.1:n.3462G>T
|
|
|
ENST00000673518.1:c.1267G>T
|
ENSP00000499889.1:p.Asp423Tyr
|
|
ENST00000304874.13:c.1345G>T
|
ENSP00000307188.9:p.Asp449Tyr
|
|
ENST00000380839.8:c.1267G>T
|
ENSP00000370219.4:p.Asp423Tyr
|
|
ENST00000395331.3:c.1285G>T
|
ENSP00000378740.3:p.Asp429Tyr
|
|
ENST00000395332.7:c.1345G>T
|
ENSP00000378741.3:p.Asp449Tyr
|
|
ENST00000450043.2:c.563+199G>T
|
ENSP00000396527.2:n.563+199G>T
|
|
ENST00000464970.1:n.548G>T
|
|
|
ENST00000488343.1:n.148-42G>T
|
|
|
ENST00000493708.5:n.826G>T
|
|
|
NM_000048.3:c.1345G>T
|
NP_000039.2:p.Asp449Tyr
|
|
NM_001024943.1:c.1345G>T
|
NP_001020114.1:p.Asp449Tyr
|
|
NM_001024944.1:c.1285G>T
|
NP_001020115.1:p.Asp429Tyr
|
|
NM_001024946.1:c.1267G>T
|
NP_001020117.1:p.Asp423Tyr
|
|
NM_000048.4:c.1345G>T
MANE Select
|
NP_000039.2:p.Asp449Tyr
|
|
NM_001024943.2:c.1345G>T
|
NP_001020114.1:p.Asp449Tyr
|
|
NM_001024944.2:c.1285G>T
|
NP_001020115.1:p.Asp429Tyr
|
|
NM_001024946.2:c.1267G>T
|
NP_001020117.1:p.Asp423Tyr
|
|