ENST00000525341.2:c.1169T>G
|
|
|
ENST00000528641.7:c.673T>G
|
ENSP00000434982.3:p.Phe225Val
|
|
ENST00000529797.2:n.1704T>G
|
|
|
ENST00000682324.1:c.469-135T>G
|
ENSP00000508017.1:n.469-135T>G
|
|
ENST00000682659.1:c.493T>G
|
ENSP00000507351.1:p.Phe165Val
|
|
ENST00000682699.1:c.862T>G
|
ENSP00000507935.1:p.Phe288Val
|
|
ENST00000683237.1:c.*2T>G
|
ENSP00000507343.1:n.*2T>G
|
|
ENST00000683856.1:c.685T>G
|
ENSP00000507979.1:p.Phe229Val
|
|
ENST00000684006.1:c.*2T>G
|
ENSP00000507269.1:n.*2T>G
|
|
ENST00000684657.1:c.682T>G
|
ENSP00000507961.1:p.Phe228Val
|
|
ENST00000279146.8:c.862T>G
MANE Select
|
ENSP00000279146.3:p.Phe288Val
|
|
ENST00000279146.7:c.862T>G
|
ENSP00000279146.3:p.Phe288Val
|
|
ENST00000528641.6:c.673T>G
|
ENSP00000434982.2:p.Phe225Val
|
|
NM_001302959.1:c.685T>G
|
NP_001289888.1:p.Phe229Val
|
|
NM_001302960.1:c.*2T>G
|
NP_001289889.1:n.*2T>G
|
|
NM_003977.3:c.862T>G
|
NP_003968.3:p.Phe288Val
|
|
XM_024448761.1:c.862T>G
|
XP_024304529.1:p.Phe288Val
|
|
NM_003977.4:c.862T>G
MANE Select
|
NP_003968.3:p.Phe288Val
|
|
NM_001302960.2:c.*2T>G
|
NP_001289889.1:n.*2T>G
|
|
NM_001302959.2:c.685T>G
|
NP_001289888.1:p.Phe229Val
|
|