ENST00000269321.12:c.*291G>C
MANE Select
|
ENSP00000269321.7:n.*291G>C
|
|
ENST00000269321.11:c.*291G>C
|
ENSP00000269321.7:n.*291G>C
|
|
ENST00000400721.8:c.*291G>C
|
ENSP00000383556.4:n.*291G>C
|
|
ENST00000541078.6:c.*291G>C
|
ENSP00000441348.2:n.*291G>C
|
|
ENST00000579121.5:c.503-1G>C
|
ENSP00000462960.1:n.503-1G>C
|
|
ENST00000580685.5:c.*291G>C
|
ENSP00000464205.1:n.*291G>C
|
|
ENST00000582520.1:n.46G>C
|
|
|
ENST00000584461.5:c.503-1G>C
|
ENSP00000463939.1:n.503-1G>C
|
|
NM_001185077.2:c.*291G>C
|
NP_001172006.1:n.*291G>C
|
|
NM_001185078.2:c.*291G>C
|
NP_001172007.1:n.*291G>C
|
|
NM_001301240.1:c.503-1G>C
|
NP_001288169.1:n.503-1G>C
|
|
NM_001301241.1:c.503-1G>C
|
NP_001288170.1:n.503-1G>C
|
|
NM_001301242.1:c.794G>C
|
NP_001288171.1:p.Arg265Thr
|
|
NM_001301243.1:c.*291G>C
|
NP_001288172.1:n.*291G>C
|
|
NM_004309.5:c.*291G>C
|
NP_004300.1:n.*291G>C
|
|
NR_125441.1:n.965G>C
|
|
|
XM_011523574.1:c.*291G>C
|
XP_011521876.1:n.*291G>C
|
|
NM_004309.6:c.*291G>C
MANE Select
|
NP_004300.1:n.*291G>C
|
|
NM_001185077.3:c.*291G>C
|
NP_001172006.1:n.*291G>C
|
|
NM_001185078.3:c.*291G>C
|
NP_001172007.1:n.*291G>C
|
|
NM_001301240.2:c.503-1G>C
|
NP_001288169.1:n.503-1G>C
|
|
NM_001301241.2:c.503-1G>C
|
NP_001288170.1:n.503-1G>C
|
|
NM_001301242.2:c.794G>C
|
NP_001288171.1:p.Arg265Thr
|
|
NM_001301243.2:c.*291G>C
|
NP_001288172.1:n.*291G>C
|
|
NR_125441.2:n.896G>C
|
|
|