ENST00000597921.6:c.509T>A
MANE Select
|
ENSP00000471974.1:p.Phe170Tyr
|
|
ENST00000346664.9:c.509T>A
|
ENSP00000264072.6:p.Phe170Tyr
|
|
ENST00000360067.8:c.506T>A
|
ENSP00000353178.4:p.Phe169Tyr
|
|
ENST00000593418.1:c.446T>A
|
ENSP00000472067.1:p.Phe149Tyr
|
|
ENST00000597312.5:n.1034T>A
|
|
|
ENST00000597921.5:c.509T>A
|
ENSP00000471974.1:p.Phe170Tyr
|
|
ENST00000597934.1:n.871T>A
|
|
|
ENST00000598803.5:n.1004T>A
|
|
|
NM_001207019.2:c.506T>A
|
NP_001193948.2:p.Phe169Tyr
|
|
NM_001220500.1:c.509T>A
|
NP_001207429.1:p.Phe170Tyr
|
|
NM_002002.4:c.509T>A
|
NP_001993.2:p.Phe170Tyr
|
|
XM_005272462.3:c.509T>A
|
XP_005272519.1:p.Phe170Tyr
|
|
XM_005272462.4:c.509T>A
|
XP_005272519.1:p.Phe170Tyr
|
|
NM_001220500.2:c.509T>A
MANE Select
|
NP_001207429.1:p.Phe170Tyr
|
|
NM_001207019.3:c.506T>A
|
NP_001193948.2:p.Phe169Tyr
|
|
NM_002002.5:c.509T>A
|
NP_001993.2:p.Phe170Tyr
|
|