|
ENST00000371224.7:c.482G>A
MANE Select
|
ENSP00000360268.2:p.Cys161Tyr
|
|
|
ENST00000371221.3:c.482G>A
|
ENSP00000360265.3:p.Cys161Tyr
|
|
|
ENST00000371224.6:c.482G>A
|
ENSP00000360268.2:p.Cys161Tyr
|
|
|
ENST00000483788.1:n.674G>A
|
|
|
|
NM_001017423.1:c.482G>A
|
NP_001017423.1:p.Cys161Tyr
|
|
|
NM_002860.3:c.482G>A
|
NP_002851.2:p.Cys161Tyr
|
|
|
XM_006717933.1:c.482G>A
|
XP_006717996.1:p.Cys161Tyr
|
|
|
XM_011540001.1:c.149G>A
|
XP_011538303.1:p.Cys50Tyr
|
|
|
NM_001323412.1:c.149G>A
|
NP_001310341.1:p.Cys50Tyr
|
|
|
NM_001323413.1:c.482G>A
|
NP_001310342.1:p.Cys161Tyr
|
|
|
NM_001323414.1:c.482G>A
|
NP_001310343.1:p.Cys161Tyr
|
|
|
NM_001323415.1:c.482G>A
|
NP_001310344.1:p.Cys161Tyr
|
|
|
NM_001323416.1:c.149G>A
|
NP_001310345.1:p.Cys50Tyr
|
|
|
NM_001323417.1:c.453+118G>A
|
NP_001310346.1:n.453+118G>A
|
|
|
NM_001323418.1:c.149G>A
|
NP_001310347.1:p.Cys50Tyr
|
|
|
NM_001323419.1:c.-78-3520G>A
|
NP_001310348.1:n.-78-3520G>A
|
|
|
XM_024448094.1:c.482G>A
|
XP_024303862.1:p.Cys161Tyr
|
|
|
XM_024448095.1:c.482G>A
|
XP_024303863.1:p.Cys161Tyr
|
|
|
XM_024448096.1:c.482G>A
|
XP_024303864.1:p.Cys161Tyr
|
|
|
XM_024448097.1:c.149G>A
|
XP_024303865.1:p.Cys50Tyr
|
|
|
NM_002860.4:c.482G>A
MANE Select
|
NP_002851.2:p.Cys161Tyr
|
|
|
NM_001017423.2:c.482G>A
|
NP_001017423.1:p.Cys161Tyr
|
|
|
NM_001323412.2:c.149G>A
|
NP_001310341.1:p.Cys50Tyr
|
|
|
NM_001323413.2:c.482G>A
|
NP_001310342.1:p.Cys161Tyr
|
|
|
NM_001323414.2:c.482G>A
|
NP_001310343.1:p.Cys161Tyr
|
|
|
NM_001323415.2:c.482G>A
|
NP_001310344.1:p.Cys161Tyr
|
|
|
NM_001323416.2:c.149G>A
|
NP_001310345.1:p.Cys50Tyr
|
|
|
NM_001323417.2:c.453+118G>A
|
NP_001310346.1:n.453+118G>A
|
|
|
NM_001323418.2:c.149G>A
|
NP_001310347.1:p.Cys50Tyr
|
|
|
NM_001323419.2:c.-78-3520G>A
|
NP_001310348.1:n.-78-3520G>A
|
|
