ENST00000304874.14:c.1162C>T
MANE Select
|
ENSP00000307188.9:p.His388Tyr
|
|
ENST00000362000.10:c.967C>T
|
ENSP00000354710.6:p.His323Tyr
|
|
ENST00000380839.9:c.1084C>T
|
ENSP00000370219.4:p.His362Tyr
|
|
ENST00000395331.4:c.1102C>T
|
ENSP00000378740.3:p.His368Tyr
|
|
ENST00000395332.8:c.1162C>T
|
ENSP00000378741.3:p.His388Tyr
|
|
ENST00000488343.2:c.148-329C>T
|
ENSP00000500864.1:n.148-329C>T
|
|
ENST00000672498.1:c.*461C>T
|
ENSP00000500227.1:n.*461C>T
|
|
ENST00000672586.1:n.1921C>T
|
|
|
ENST00000672676.1:n.2186C>T
|
|
|
ENST00000673149.1:n.974C>T
|
|
|
ENST00000673350.1:n.3279C>T
|
|
|
ENST00000673518.1:c.1084C>T
|
ENSP00000499889.1:p.His362Tyr
|
|
ENST00000304874.13:c.1162C>T
|
ENSP00000307188.9:p.His388Tyr
|
|
ENST00000380839.8:c.1084C>T
|
ENSP00000370219.4:p.His362Tyr
|
|
ENST00000395331.3:c.1102C>T
|
ENSP00000378740.3:p.His368Tyr
|
|
ENST00000395332.7:c.1162C>T
|
ENSP00000378741.3:p.His388Tyr
|
|
ENST00000450043.2:c.475C>T
|
ENSP00000396527.2:p.His159Tyr
|
|
ENST00000464970.1:n.365C>T
|
|
|
ENST00000488343.1:n.148-329C>T
|
|
|
ENST00000493708.5:n.643C>T
|
|
|
NM_000048.3:c.1162C>T
|
NP_000039.2:p.His388Tyr
|
|
NM_001024943.1:c.1162C>T
|
NP_001020114.1:p.His388Tyr
|
|
NM_001024944.1:c.1102C>T
|
NP_001020115.1:p.His368Tyr
|
|
NM_001024946.1:c.1084C>T
|
NP_001020117.1:p.His362Tyr
|
|
NM_000048.4:c.1162C>T
MANE Select
|
NP_000039.2:p.His388Tyr
|
|
NM_001024943.2:c.1162C>T
|
NP_001020114.1:p.His388Tyr
|
|
NM_001024944.2:c.1102C>T
|
NP_001020115.1:p.His368Tyr
|
|
NM_001024946.2:c.1084C>T
|
NP_001020117.1:p.His362Tyr
|
|