ENST00000534624.6:c.1516G>T
MANE Select
|
ENSP00000432083.1:p.Asp506Tyr
|
|
ENST00000227378.7:c.1516G>T
|
ENSP00000227378.3:p.Asp506Tyr
|
|
ENST00000453788.6:c.1387+129G>T
|
ENSP00000404372.2:n.1387+129G>T
|
|
ENST00000524552.5:c.289G>T
|
ENSP00000435908.1:p.Asp97Tyr
|
|
ENST00000526110.5:c.1459G>T
|
ENSP00000433584.1:p.Asp487Tyr
|
|
ENST00000526686.1:c.172G>T
|
ENSP00000435019.1:p.Asp58Tyr
|
|
ENST00000532091.1:n.1491G>T
|
|
|
ENST00000532636.5:c.1516G>T
|
ENSP00000437125.1:p.Asp506Tyr
|
|
ENST00000533540.5:c.1078G>T
|
ENSP00000437189.1:p.Asp360Tyr
|
|
ENST00000534319.5:c.808G>T
|
ENSP00000433316.1:p.Asp270Tyr
|
|
ENST00000534624.5:c.1516G>T
|
ENSP00000432083.1:p.Asp506Tyr
|
|
NM_006597.5:c.1516G>T
|
NP_006588.1:p.Asp506Tyr
|
|
NM_153201.3:c.1387+129G>T
|
NP_694881.1:n.1387+129G>T
|
|
XM_011542798.1:c.1516G>T
|
XP_011541100.1:p.Asp506Tyr
|
|
NM_006597.6:c.1516G>T
MANE Select
|
NP_006588.1:p.Asp506Tyr
|
|
NM_153201.4:c.1387+129G>T
|
NP_694881.1:n.1387+129G>T
|
|