ENST00000269321.12:c.517G>C
MANE Select
|
ENSP00000269321.7:p.Gly173Arg
|
|
ENST00000269321.11:c.517G>C
|
ENSP00000269321.7:p.Gly173Arg
|
|
ENST00000400721.8:c.416-31G>C
|
ENSP00000383556.4:n.416-31G>C
|
|
ENST00000541078.6:c.517G>C
|
ENSP00000441348.2:p.Gly173Arg
|
|
ENST00000579121.5:c.502+15G>C
|
ENSP00000462960.1:n.502+15G>C
|
|
ENST00000580033.5:c.*161G>C
|
ENSP00000463530.1:n.*161G>C
|
|
ENST00000580685.5:c.517G>C
|
ENSP00000464205.1:p.Gly173Arg
|
|
ENST00000581876.5:c.292G>C
|
ENSP00000461956.1:p.Gly98Arg
|
|
ENST00000582984.5:n.719G>C
|
|
|
ENST00000583868.5:c.436-31G>C
|
ENSP00000462209.1:n.436-31G>C
|
|
ENST00000584461.5:c.502+15G>C
|
ENSP00000463939.1:n.502+15G>C
|
|
NM_001185077.2:c.517G>C
|
NP_001172006.1:p.Gly173Arg
|
|
NM_001185078.2:c.416-31G>C
|
NP_001172007.1:n.416-31G>C
|
|
NM_001301240.1:c.502+15G>C
|
NP_001288169.1:n.502+15G>C
|
|
NM_001301241.1:c.502+15G>C
|
NP_001288170.1:n.502+15G>C
|
|
NM_001301242.1:c.436-31G>C
|
NP_001288171.1:n.436-31G>C
|
|
NM_001301243.1:c.652G>C
|
NP_001288172.1:p.Gly218Arg
|
|
NM_004309.5:c.517G>C
|
NP_004300.1:p.Gly173Arg
|
|
NR_125441.1:n.576G>C
|
|
|
XM_011523574.1:c.652G>C
|
XP_011521876.1:p.Gly218Arg
|
|
NM_004309.6:c.517G>C
MANE Select
|
NP_004300.1:p.Gly173Arg
|
|
NM_001185077.3:c.517G>C
|
NP_001172006.1:p.Gly173Arg
|
|
NM_001185078.3:c.416-31G>C
|
NP_001172007.1:n.416-31G>C
|
|
NM_001301240.2:c.502+15G>C
|
NP_001288169.1:n.502+15G>C
|
|
NM_001301241.2:c.502+15G>C
|
NP_001288170.1:n.502+15G>C
|
|
NM_001301242.2:c.436-31G>C
|
NP_001288171.1:n.436-31G>C
|
|
NM_001301243.2:c.652G>C
|
NP_001288172.1:p.Gly218Arg
|
|
NR_125441.2:n.507G>C
|
|
|