ENST00000525341.2:c.1144G>C
|
|
|
ENST00000528641.7:c.648G>C
|
ENSP00000434982.3:p.Trp216Cys
|
|
ENST00000529797.2:n.1679G>C
|
|
|
ENST00000682324.1:c.469-160G>C
|
ENSP00000508017.1:n.469-160G>C
|
|
ENST00000682659.1:c.468G>C
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ENSP00000507351.1:p.Trp156Cys
|
|
ENST00000682699.1:c.837G>C
|
ENSP00000507935.1:p.Trp279Cys
|
|
ENST00000683237.1:c.829G>C
|
ENSP00000507343.1:p.Glu277Gln
|
|
ENST00000683856.1:c.660G>C
|
ENSP00000507979.1:p.Trp220Cys
|
|
ENST00000684006.1:c.826G>C
|
ENSP00000507269.1:p.Glu276Gln
|
|
ENST00000684657.1:c.657G>C
|
ENSP00000507961.1:p.Trp219Cys
|
|
ENST00000279146.8:c.837G>C
MANE Select
|
ENSP00000279146.3:p.Trp279Cys
|
|
ENST00000279146.7:c.837G>C
|
ENSP00000279146.3:p.Trp279Cys
|
|
ENST00000528641.6:c.648G>C
|
ENSP00000434982.2:p.Trp216Cys
|
|
NM_001302959.1:c.660G>C
|
NP_001289888.1:p.Trp220Cys
|
|
NM_001302960.1:c.829G>C
|
NP_001289889.1:p.Glu277Gln
|
|
NM_003977.3:c.837G>C
|
NP_003968.3:p.Trp279Cys
|
|
XM_024448761.1:c.837G>C
|
XP_024304529.1:p.Trp279Cys
|
|
NM_003977.4:c.837G>C
MANE Select
|
NP_003968.3:p.Trp279Cys
|
|
NM_001302960.2:c.829G>C
|
NP_001289889.1:p.Glu277Gln
|
|
NM_001302959.2:c.660G>C
|
NP_001289888.1:p.Trp220Cys
|
|