ENST00000558428.6:c.216G>C
|
ENSP00000454165.2:p.Glu72Asp
|
|
ENST00000558739.2:c.486G>C
|
ENSP00000453684.2:p.Glu162Asp
|
|
ENST00000558827.2:c.216G>C
|
ENSP00000452767.2:p.Glu72Asp
|
|
ENST00000559460.6:c.486G>C
|
ENSP00000453082.2:p.Glu162Asp
|
|
ENST00000560424.2:c.801G>C
|
ENSP00000455540.2:p.Glu267Asp
|
|
ENST00000327367.9:c.801G>C
MANE Select
|
ENSP00000332973.4:p.Glu267Asp
|
|
ENST00000679624.1:c.486G>C
|
ENSP00000505445.1:p.Glu162Asp
|
|
ENST00000680689.1:n.504G>C
|
|
|
ENST00000681239.1:c.486G>C
|
ENSP00000505641.1:p.Glu162Asp
|
|
ENST00000327367.8:c.801G>C
|
ENSP00000332973.4:p.Glu267Asp
|
|
ENST00000439724.7:c.669G>C
|
ENSP00000401133.3:p.Glu223Asp
|
|
ENST00000537194.6:c.216G>C
|
ENSP00000445348.2:p.Glu72Asp
|
|
ENST00000540846.6:c.486G>C
|
ENSP00000437757.2:p.Glu162Asp
|
|
ENST00000558428.5:c.216G>C
|
ENSP00000454165.1:p.Glu72Asp
|
|
ENST00000558827.1:c.216G>C
|
ENSP00000452767.1:p.Glu72Asp
|
|
ENST00000558894.5:c.486G>C
|
ENSP00000458060.1:p.Glu162Asp
|
|
ENST00000560402.1:n.282+6799G>C
|
|
|
NM_001145102.1:c.486G>C
|
NP_001138574.1:p.Glu162Asp
|
|
NM_001145103.1:c.669G>C
|
NP_001138575.1:p.Glu223Asp
|
|
NM_001145104.1:c.216G>C
|
NP_001138576.1:p.Glu72Asp
|
|
NM_005902.3:c.801G>C
|
NP_005893.1:p.Glu267Asp
|
|
XM_011521559.1:c.669G>C
|
XP_011519861.1:p.Glu223Asp
|
|
XM_011521560.1:c.654G>C
|
XP_011519862.1:p.Glu218Asp
|
|
XM_011521559.3:c.669G>C
|
XP_011519861.1:p.Glu223Asp
|
|
NM_005902.4:c.801G>C
MANE Select
|
NP_005893.1:p.Glu267Asp
|
|
NM_001145102.2:c.486G>C
|
NP_001138574.1:p.Glu162Asp
|
|
NM_001145103.2:c.669G>C
|
NP_001138575.1:p.Glu223Asp
|
|
NM_001145104.2:c.216G>C
|
NP_001138576.1:p.Glu72Asp
|
|