ENST00000525341.2:c.534G>T
|
|
|
ENST00000528641.7:c.368G>T
|
ENSP00000434982.3:p.Gly123Val
|
|
ENST00000529797.2:n.1069G>T
|
|
|
ENST00000682324.1:c.468+671G>T
|
ENSP00000508017.1:n.468+671G>T
|
|
ENST00000682659.1:c.188G>T
|
ENSP00000507351.1:p.Gly63Val
|
|
ENST00000682699.1:c.557G>T
|
ENSP00000507935.1:p.Gly186Val
|
|
ENST00000683237.1:c.557G>T
|
ENSP00000507343.1:p.Gly186Val
|
|
ENST00000683856.1:c.380G>T
|
ENSP00000507979.1:p.Gly127Val
|
|
ENST00000684006.1:c.557G>T
|
ENSP00000507269.1:p.Gly186Val
|
|
ENST00000684657.1:c.377G>T
|
ENSP00000507961.1:p.Gly126Val
|
|
ENST00000279146.8:c.557G>T
MANE Select
|
ENSP00000279146.3:p.Gly186Val
|
|
ENST00000279146.7:c.557G>T
|
ENSP00000279146.3:p.Gly186Val
|
|
ENST00000525341.1:c.209G>T
|
ENSP00000476993.1:p.Gly70Val
|
|
ENST00000528641.6:c.368G>T
|
ENSP00000434982.2:p.Gly123Val
|
|
NM_001302959.1:c.380G>T
|
NP_001289888.1:p.Gly127Val
|
|
NM_001302960.1:c.557G>T
|
NP_001289889.1:p.Gly186Val
|
|
NM_003977.3:c.557G>T
|
NP_003968.3:p.Gly186Val
|
|
XM_024448761.1:c.557G>T
|
XP_024304529.1:p.Gly186Val
|
|
NM_003977.4:c.557G>T
MANE Select
|
NP_003968.3:p.Gly186Val
|
|
NM_001302960.2:c.557G>T
|
NP_001289889.1:p.Gly186Val
|
|
NM_001302959.2:c.380G>T
|
NP_001289888.1:p.Gly127Val
|
|