|
ENST00000697700.2:c.1525G>T
|
ENSP00000513407.2:p.Gly509Cys
|
|
|
ENST00000697701.1:c.1570G>T
|
ENSP00000513408.1:p.Gly524Cys
|
|
|
ENST00000697702.1:c.1522G>T
|
ENSP00000513409.1:p.Gly508Cys
|
|
|
ENST00000704363.1:c.1501G>T
|
ENSP00000515871.1:p.Gly501Cys
|
|
|
ENST00000687212.1:c.1591G>T
MANE Select
|
ENSP00000509890.1:p.Gly531Cys
|
|
|
ENST00000262811.10:c.1504G>T
|
ENSP00000262811.4:p.Gly502Cys
|
|
|
NM_015016.1:c.1504G>T
|
NP_055831.1:p.Gly502Cys
|
|
|
XM_005259822.2:c.2038G>T
|
XP_005259879.2:p.Gly680Cys
|
|
|
XM_005259823.2:c.1543G>T
|
XP_005259880.1:p.Gly515Cys
|
|
|
XM_005259824.2:c.1525G>T
|
XP_005259881.1:p.Gly509Cys
|
|
|
XM_005259825.2:c.1522G>T
|
XP_005259882.1:p.Gly508Cys
|
|
|
XM_005259826.2:c.1519G>T
|
XP_005259883.1:p.Gly507Cys
|
|
|
XM_005259827.1:c.1522G>T
|
XP_005259884.1:p.Gly508Cys
|
|
|
XM_006722693.2:c.2062G>T
|
XP_006722756.2:p.Gly688Cys
|
|
|
XM_006722694.2:c.2059G>T
|
XP_006722757.2:p.Gly687Cys
|
|
|
XM_006722695.2:c.2041G>T
|
XP_006722758.2:p.Gly681Cys
|
|
|
XM_006722696.2:c.2062G>T
|
XP_006722759.2:p.Gly688Cys
|
|
|
XM_006722697.2:c.2041G>T
|
XP_006722760.2:p.Gly681Cys
|
|
|
XM_006722698.2:c.1279G>T
|
XP_006722761.1:p.Gly427Cys
|
|
|
XM_006722699.2:c.1807G>T
|
XP_006722762.2:p.Gly603Cys
|
|
|
XM_006722700.2:c.1519G>T
|
XP_006722763.1:p.Gly507Cys
|
|
|
XM_011527823.1:c.1615G>T
|
XP_011526125.1:p.Gly539Cys
|
|
|
XM_005259823.3:c.1543G>T
|
XP_005259880.1:p.Gly515Cys
|
|
|
XM_005259826.3:c.1519G>T
|
XP_005259883.1:p.Gly507Cys
|
|
|
XM_005259827.3:c.1522G>T
|
XP_005259884.1:p.Gly508Cys
|
|
|
XM_006722700.3:c.1519G>T
|
XP_006722763.1:p.Gly507Cys
|
|
|
XM_017026506.1:c.1804G>T
|
XP_016881995.1:p.Gly602Cys
|
|
|
XM_017026507.1:c.1786G>T
|
XP_016881996.1:p.Gly596Cys
|
|
|
XM_017026508.1:c.1783G>T
|
XP_016881997.1:p.Gly595Cys
|
|
|
XM_017026509.1:c.1807G>T
|
XP_016881998.1:p.Gly603Cys
|
|
|
XM_017026510.2:c.1786G>T
|
XP_016881999.1:p.Gly596Cys
|
|
|
XM_017026511.1:c.1591G>T
|
XP_016882000.1:p.Gly531Cys
|
|
|
XM_017026512.1:c.1504G>T
|
XP_016882001.1:p.Gly502Cys
|
|
|
XM_017026513.1:c.1501G>T
|
XP_016882002.1:p.Gly501Cys
|
|
|
XM_017026514.1:c.1279G>T
|
XP_016882003.1:p.Gly427Cys
|
|
|
XM_017026515.1:c.1279G>T
|
XP_016882004.1:p.Gly427Cys
|
|
|
XM_017026516.1:c.1804G>T
|
XP_016882005.1:p.Gly602Cys
|
|
|
NM_015016.2:c.1504G>T
|
NP_055831.1:p.Gly502Cys
|
|
|
NM_001393501.1:c.1615G>T
|
NP_001380430.1:p.Gly539Cys
|
|
|
NM_001393502.1:c.1594G>T
|
NP_001380431.1:p.Gly532Cys
|
|
|
NM_001393503.1:c.1591G>T
|
NP_001380432.1:p.Gly531Cys
|
|
|
NM_001393504.1:c.1591G>T
MANE Select
|
NP_001380433.1:p.Gly531Cys
|
|
|
NM_001393505.1:c.1588G>T
|
NP_001380434.1:p.Gly530Cys
|
|
|
NM_001393506.1:c.1543G>T
|
NP_001380435.1:p.Gly515Cys
|
|
|
NM_001393507.1:c.1570G>T
|
NP_001380436.1:p.Gly524Cys
|
|
|
NM_001393508.1:c.1525G>T
|
NP_001380437.1:p.Gly509Cys
|
|
|
NM_001393509.1:c.1522G>T
|
NP_001380438.1:p.Gly508Cys
|
|
|
NM_001393510.1:c.1522G>T
|
NP_001380439.1:p.Gly508Cys
|
|
|
NM_001393511.1:c.1519G>T
|
NP_001380440.1:p.Gly507Cys
|
|
|
NM_001393512.1:c.1522G>T
|
NP_001380441.1:p.Gly508Cys
|
|
|
NM_001393513.1:c.1543G>T
|
NP_001380442.1:p.Gly515Cys
|
|
|
NM_001393514.1:c.1504G>T
|
NP_001380443.1:p.Gly502Cys
|
|
|
NM_001393515.1:c.1501G>T
|
NP_001380444.1:p.Gly501Cys
|
|
|
NM_001393516.1:c.1525G>T
|
NP_001380445.1:p.Gly509Cys
|
|
|
NM_001393517.1:c.1522G>T
|
NP_001380446.1:p.Gly508Cys
|
|
|
NM_001393518.1:c.1522G>T
|
NP_001380447.1:p.Gly508Cys
|
|
|
NM_001393519.1:c.1519G>T
|
NP_001380448.1:p.Gly507Cys
|
|
|
NM_001393520.1:c.1501G>T
|
NP_001380449.1:p.Gly501Cys
|
|
|
NM_001393521.1:c.1477G>T
|
NP_001380450.1:p.Gly493Cys
|
|
