ENST00000696964.1:c.481-4393A>G
|
ENSP00000513003.1:n.481-4393A>G
|
|
ENST00000269197.12:c.478-4393A>G
MANE Select
|
ENSP00000269197.4:n.478-4393A>G
|
|
ENST00000586327.6:n.548-4393A>G
|
|
|
ENST00000590189.6:n.485-4393A>G
|
|
|
ENST00000592288.6:c.481-4393A>G
|
ENSP00000465053.1:n.481-4393A>G
|
|
ENST00000592541.6:c.*421-4393A>G
|
ENSP00000466655.2:n.*421-4393A>G
|
|
ENST00000593195.6:c.690-4393A>G
|
ENSP00000466073.1:n.690-4393A>G
|
|
ENST00000642541.1:c.310-4393A>G
|
ENSP00000493665.1:n.310-4393A>G
|
|
ENST00000681521.1:c.478-4393A>G
|
ENSP00000506037.1:n.478-4393A>G
|
|
ENST00000269197.9:c.478-4393A>G
|
ENSP00000269197.4:n.478-4393A>G
|
|
ENST00000586596.5:c.447-4393A>G
|
|
|
ENST00000590189.5:c.469-4393A>G
|
ENSP00000468024.1:n.469-4393A>G
|
|
ENST00000592288.5:c.481-4393A>G
|
ENSP00000465053.1:n.481-4393A>G
|
|
ENST00000592541.5:c.*418-4393A>G
|
ENSP00000466655.1:n.*418-4393A>G
|
|
ENST00000593235.1:c.*283-4393A>G
|
ENSP00000467907.1:n.*283-4393A>G
|
|
NM_030632.1:c.478-4393A>G
|
NP_085135.1:n.478-4393A>G
|
|
XM_005258356.1:c.481-4393A>G
|
XP_005258413.1:n.481-4393A>G
|
|
XM_011526205.1:c.454-4393A>G
|
XP_011524507.1:n.454-4393A>G
|
|
XM_011526206.1:c.400-4393A>G
|
XP_011524508.1:n.400-4393A>G
|
|
XM_011526207.1:c.400-4393A>G
|
XP_011524509.1:n.400-4393A>G
|
|
XM_011526208.1:c.481-4393A>G
|
XP_011524510.1:n.481-4393A>G
|
|
XM_011526209.1:c.310-4393A>G
|
XP_011524511.1:n.310-4393A>G
|
|
XM_011526210.1:c.310-4393A>G
|
XP_011524512.1:n.310-4393A>G
|
|
XM_011526211.1:c.310-4393A>G
|
XP_011524513.1:n.310-4393A>G
|
|
XM_011526212.1:c.310-4393A>G
|
XP_011524514.1:n.310-4393A>G
|
|
XM_011526213.1:c.310-4393A>G
|
XP_011524515.1:n.310-4393A>G
|
|
XM_011526214.1:c.310-4393A>G
|
XP_011524516.1:n.310-4393A>G
|
|
NM_030632.2:c.478-4393A>G
|
NP_085135.1:n.478-4393A>G
|
|
XM_011526205.2:c.454-4393A>G
|
XP_011524507.1:n.454-4393A>G
|
|
XM_011526206.2:c.400-4393A>G
|
XP_011524508.1:n.400-4393A>G
|
|
XM_011526213.2:c.310-4393A>G
|
XP_011524515.1:n.310-4393A>G
|
|
XM_017026012.1:c.400-4393A>G
|
XP_016881501.1:n.400-4393A>G
|
|
XM_017026013.1:c.310-4393A>G
|
XP_016881502.1:n.310-4393A>G
|
|
XM_017026014.2:c.310-4393A>G
|
XP_016881503.1:n.310-4393A>G
|
|
XM_024451269.1:c.310-4393A>G
|
XP_024307037.1:n.310-4393A>G
|
|
NM_030632.3:c.478-4393A>G
MANE Select
|
NP_085135.1:n.478-4393A>G
|
|