ENST00000269321.12:c.471G>C
MANE Select
|
ENSP00000269321.7:p.Glu157Asp
|
|
ENST00000269321.11:c.471G>C
|
ENSP00000269321.7:p.Glu157Asp
|
|
ENST00000400721.8:c.416-77G>C
|
ENSP00000383556.4:n.416-77G>C
|
|
ENST00000541078.6:c.471G>C
|
ENSP00000441348.2:p.Glu157Asp
|
|
ENST00000579121.5:c.471G>C
|
ENSP00000462960.1:p.Glu157Asp
|
|
ENST00000580033.5:c.*115G>C
|
ENSP00000463530.1:n.*115G>C
|
|
ENST00000580685.5:c.471G>C
|
ENSP00000464205.1:p.Glu157Asp
|
|
ENST00000581876.5:c.246G>C
|
ENSP00000461956.1:p.Glu82Asp
|
|
ENST00000582984.5:n.673G>C
|
|
|
ENST00000583791.1:n.335G>C
|
|
|
ENST00000583868.5:c.435+36G>C
|
ENSP00000462209.1:n.435+36G>C
|
|
ENST00000584461.5:c.471G>C
|
ENSP00000463939.1:p.Glu157Asp
|
|
NM_001185077.2:c.471G>C
|
NP_001172006.1:p.Glu157Asp
|
|
NM_001185078.2:c.416-77G>C
|
NP_001172007.1:n.416-77G>C
|
|
NM_001301240.1:c.471G>C
|
NP_001288169.1:p.Glu157Asp
|
|
NM_001301241.1:c.471G>C
|
NP_001288170.1:p.Glu157Asp
|
|
NM_001301242.1:c.435+36G>C
|
NP_001288171.1:n.435+36G>C
|
|
NM_001301243.1:c.606G>C
|
NP_001288172.1:p.Glu202Asp
|
|
NM_004309.5:c.471G>C
|
NP_004300.1:p.Glu157Asp
|
|
NR_125441.1:n.530G>C
|
|
|
XM_011523574.1:c.606G>C
|
XP_011521876.1:p.Glu202Asp
|
|
NM_004309.6:c.471G>C
MANE Select
|
NP_004300.1:p.Glu157Asp
|
|
NM_001185077.3:c.471G>C
|
NP_001172006.1:p.Glu157Asp
|
|
NM_001185078.3:c.416-77G>C
|
NP_001172007.1:n.416-77G>C
|
|
NM_001301240.2:c.471G>C
|
NP_001288169.1:p.Glu157Asp
|
|
NM_001301241.2:c.471G>C
|
NP_001288170.1:p.Glu157Asp
|
|
NM_001301242.2:c.435+36G>C
|
NP_001288171.1:n.435+36G>C
|
|
NM_001301243.2:c.606G>C
|
NP_001288172.1:p.Glu202Asp
|
|
NR_125441.2:n.461G>C
|
|
|