ENST00000405460.9:c.9097G>C
MANE Select
|
ENSP00000384582.2:p.Asp3033His
|
|
ENST00000639431.1:c.265+36132G>C
|
ENSP00000491057.1:n.265+36132G>C
|
|
ENST00000639473.1:n.4556G>C
|
|
|
ENST00000640012.1:c.2904G>C
|
|
|
ENST00000640374.1:n.2241G>C
|
|
|
ENST00000640779.1:c.3826G>C
|
|
|
ENST00000405460.6:c.9097G>C
|
ENSP00000384582.2:p.Asp3033His
|
|
ENST00000509621.1:c.1794G>C
|
|
|
NM_032119.3:c.9097G>C
|
NP_115495.3:p.Asp3033His
|
|
NR_003149.1:n.9110G>C
|
|
|
XM_011543675.1:c.9094G>C
|
XP_011541977.1:p.Asp3032His
|
|
XM_011543676.1:c.9016G>C
|
XP_011541978.1:p.Asp3006His
|
|
XM_011543677.1:c.6400G>C
|
XP_011541979.1:p.Asp2134His
|
|
XM_011543678.1:c.9097G>C
|
XP_011541980.1:p.Asp3033His
|
|
XM_011543679.1:c.9097G>C
|
XP_011541981.1:p.Asp3033His
|
|
NM_032119.4:c.9097G>C
MANE Select
|
NP_115495.3:p.Asp3033His
|
|
XM_017009963.2:c.9118G>C
|
XP_016865452.1:p.Asp3040His
|
|
XM_017009964.2:c.9115G>C
|
XP_016865453.1:p.Asp3039His
|
|
XM_017009965.1:c.9115G>C
|
XP_016865454.1:p.Asp3039His
|
|
XM_017009966.2:c.9037G>C
|
XP_016865455.1:p.Asp3013His
|
|
XM_017009967.1:c.9022G>C
|
XP_016865456.1:p.Asp3008His
|
|
XM_017009968.2:c.9118G>C
|
XP_016865457.1:p.Asp3040His
|
|
XM_017009969.2:c.9118G>C
|
XP_016865458.1:p.Asp3040His
|
|
XM_017009970.2:c.9118G>C
|
XP_016865459.1:p.Asp3040His
|
|
XM_017009971.2:c.9118G>C
|
XP_016865460.1:p.Asp3040His
|
|
XM_017009972.1:c.2236G>C
|
XP_016865461.1:p.Asp746His
|
|
XM_017009973.1:c.2215G>C
|
XP_016865462.1:p.Asp739His
|
|
XM_017009974.2:c.9118G>C
|
XP_016865463.1:p.Asp3040His
|
|
NR_003149.2:n.9113G>C
|
|
|