ENST00000302804.12:c.-38G>T
MANE Select
|
ENSP00000302898.6:n.-38G>T
|
|
ENST00000302804.11:c.-38G>T
|
ENSP00000302898.6:n.-38G>T
|
|
ENST00000415300.6:c.1+97G>T
|
ENSP00000407162.1:n.1+97G>T
|
|
ENST00000448930.5:c.-45+91G>T
|
ENSP00000406798.2:n.-45+91G>T
|
|
ENST00000601799.5:c.-38G>T
|
ENSP00000468918.1:n.-38G>T
|
|
NM_001015878.1:c.-38G>T
|
NP_001015878.1:n.-38G>T
|
|
NM_001015879.1:c.1+97G>T
|
NP_001015879.1:n.1+97G>T
|
|
NM_003160.2:c.-45+92G>T
|
NP_003151.2:n.-45+92G>T
|
|
XR_430209.2:n.852G>T
|
|
|
XR_430209.3:n.895G>T
|
|
|
NM_001015878.2:c.-38G>T
MANE Select
|
NP_001015878.1:n.-38G>T
|
|
NM_001015879.2:c.1+97G>T
|
NP_001015879.1:n.1+97G>T
|
|
NM_003160.3:c.-45+92G>T
|
NP_003151.2:n.-45+92G>T
|
|