ENST00000698881.1:c.1036G>T
|
ENSP00000514003.1:p.Gly346Cys
|
|
ENST00000418331.7:c.694G>T
MANE Select
|
ENSP00000400010.2:p.Gly232Cys
|
|
ENST00000418331.6:c.694G>T
|
ENSP00000400010.2:p.Gly232Cys
|
|
ENST00000440289.6:c.694G>T
|
ENSP00000409733.2:p.Gly232Cys
|
|
ENST00000527952.1:c.430G>T
|
ENSP00000435618.1:p.Gly144Cys
|
|
ENST00000613246.4:c.694G>T
|
ENSP00000477933.1:p.Gly232Cys
|
|
ENST00000615445.4:c.694G>T
|
ENSP00000479342.1:p.Gly232Cys
|
|
NM_001098503.1:c.694G>T
|
NP_001091973.1:p.Gly232Cys
|
|
NM_002843.3:c.694G>T
|
NP_002834.3:p.Gly232Cys
|
|
XM_011520249.1:c.727G>T
|
XP_011518551.1:p.Gly243Cys
|
|
XR_930883.1:n.1044G>T
|
|
|
XM_017018083.1:c.772G>T
|
XP_016873572.1:p.Gly258Cys
|
|
XM_017018084.1:c.715G>T
|
XP_016873573.1:p.Gly239Cys
|
|
XM_017018085.1:c.646G>T
|
XP_016873574.1:p.Gly216Cys
|
|
XR_930883.2:n.1103G>T
|
|
|
NM_002843.4:c.694G>T
MANE Select
|
NP_002834.3:p.Gly232Cys
|
|
NM_001098503.2:c.694G>T
|
NP_001091973.1:p.Gly232Cys
|
|