|
NM_032119.4:c.5311C>T
MANE Select
|
NP_115495.3:p.Gln1771Ter
|
|
ENST00000405460.9:c.5311C>T
MANE Select
|
ENSP00000384582.2:p.Gln1771Ter
|
|
NM_032119.3:c.5311C>T
|
NP_115495.3:p.Gln1771Ter
|
|
NR_003149.1:n.5407C>T
|
|
|
NR_003149.2:n.5410C>T
|
|
|
ENST00000405460.6:c.5311C>T
|
ENSP00000384582.2:p.Gln1771Ter
|
|
ENST00000450321.2:n.646C>T
|
|
|
ENST00000639431.1:c.133C>T
|
ENSP00000491057.1:p.Gln45Ter
|
|
ENST00000639473.1:n.770C>T
|
|
|
ENST00000640403.1:c.2602C>T
|
ENSP00000492531.1:p.Gln868Ter
|
|
ENST00000640779.1:c.126C>T
|
|
|
XM_011543675.1:c.5311C>T
|
XP_011541977.1:p.Gln1771Ter
|
|
XM_011543676.1:c.5311C>T
|
XP_011541978.1:p.Gln1771Ter
|
|
XM_011543677.1:c.2614C>T
|
XP_011541979.1:p.Gln872Ter
|
|
XM_011543678.1:c.5311C>T
|
XP_011541980.1:p.Gln1771Ter
|
|
XM_011543679.1:c.5311C>T
|
XP_011541981.1:p.Gln1771Ter
|
|
XM_017009963.2:c.5311C>T
|
XP_016865452.1:p.Gln1771Ter
|
|
XM_017009964.2:c.5311C>T
|
XP_016865453.1:p.Gln1771Ter
|
|
XM_017009965.1:c.5308C>T
|
XP_016865454.1:p.Gln1770Ter
|
|
XM_017009966.2:c.5311C>T
|
XP_016865455.1:p.Gln1771Ter
|
|
XM_017009967.1:c.5215C>T
|
XP_016865456.1:p.Gln1739Ter
|
|
XM_017009968.2:c.5311C>T
|
XP_016865457.1:p.Gln1771Ter
|
|
XM_017009969.2:c.5311C>T
|
XP_016865458.1:p.Gln1771Ter
|
|
XM_017009970.2:c.5311C>T
|
XP_016865459.1:p.Gln1771Ter
|
|
XM_017009971.2:c.5311C>T
|
XP_016865460.1:p.Gln1771Ter
|
|
XM_017009973.1:c.-1486C>T
|
XP_016865462.1:n.-1486C>T
|
|
XM_017009974.2:c.5311C>T
|
XP_016865463.1:p.Gln1771Ter
|