ENST00000312428.11:c.10754T>A
MANE Select
|
ENSP00000311273.6:p.Phe3585Tyr
|
|
ENST00000312428.10:c.10754T>A
|
ENSP00000311273.6:p.Phe3585Tyr
|
|
ENST00000409063.5:c.203T>A
|
ENSP00000386912.1:p.Phe68Tyr
|
|
NM_018897.2:c.10754T>A
|
NP_061720.2:p.Phe3585Tyr
|
|
XM_011511487.1:c.10754T>A
|
XP_011509789.1:p.Phe3585Tyr
|
|
XM_011511488.1:c.10634T>A
|
XP_011509790.1:p.Phe3545Tyr
|
|
XM_011511489.1:c.10616T>A
|
XP_011509791.1:p.Phe3539Tyr
|
|
XM_011511490.1:c.10529T>A
|
XP_011509792.1:p.Phe3510Tyr
|
|
XM_011511496.1:c.6398T>A
|
XP_011509798.1:p.Phe2133Tyr
|
|
XM_011511497.1:c.5126T>A
|
XP_011509799.1:p.Phe1709Tyr
|
|
XM_011511488.3:c.10634T>A
|
XP_011509790.1:p.Phe3545Tyr
|
|
XM_011511489.2:c.10616T>A
|
XP_011509791.1:p.Phe3539Tyr
|
|
XM_011511490.3:c.10529T>A
|
XP_011509792.1:p.Phe3510Tyr
|
|
XM_011511497.2:c.5126T>A
|
XP_011509799.1:p.Phe1709Tyr
|
|
XM_017004504.2:c.10481T>A
|
XP_016859993.1:p.Phe3494Tyr
|
|
NM_018897.3:c.10754T>A
MANE Select
|
NP_061720.2:p.Phe3585Tyr
|
|