ENST00000525341.2:c.1286A>T
|
|
|
ENST00000528641.7:c.790A>T
|
ENSP00000434982.3:p.Ile264Phe
|
|
ENST00000529797.2:n.1821A>T
|
|
|
ENST00000682324.1:c.469-18A>T
|
ENSP00000508017.1:n.469-18A>T
|
|
ENST00000682659.1:c.610A>T
|
ENSP00000507351.1:p.Ile204Phe
|
|
ENST00000683237.1:c.*119A>T
|
ENSP00000507343.1:n.*119A>T
|
|
ENST00000683856.1:c.802A>T
|
ENSP00000507979.1:p.Ile268Phe
|
|
ENST00000684006.1:c.*119A>T
|
ENSP00000507269.1:n.*119A>T
|
|
ENST00000684657.1:c.799A>T
|
ENSP00000507961.1:p.Ile267Phe
|
|
ENST00000279146.8:c.979A>T
MANE Select
|
ENSP00000279146.3:p.Ile327Phe
|
|
ENST00000279146.7:c.979A>T
|
ENSP00000279146.3:p.Ile327Phe
|
|
NM_001302959.1:c.802A>T
|
NP_001289888.1:p.Ile268Phe
|
|
NM_001302960.1:c.*119A>T
|
NP_001289889.1:n.*119A>T
|
|
NM_003977.3:c.979A>T
|
NP_003968.3:p.Ile327Phe
|
|
XM_024448761.1:c.979A>T
|
XP_024304529.1:p.Ile327Phe
|
|
NM_003977.4:c.979A>T
MANE Select
|
NP_003968.3:p.Ile327Phe
|
|
NM_001302960.2:c.*119A>T
|
NP_001289889.1:n.*119A>T
|
|
NM_001302959.2:c.802A>T
|
NP_001289888.1:p.Ile268Phe
|
|