ENST00000460843.6:c.1971G>T
MANE Select
|
ENSP00000417980.1:p.Gln657His
|
|
ENST00000636027.1:c.1857G>T
|
ENSP00000489961.1:p.Gln619His
|
|
ENST00000637161.1:c.1878G>T
|
ENSP00000490328.1:p.Gln626His
|
|
ENST00000637261.1:c.2011G>T
|
ENSP00000490815.1:n.2011G>T
|
|
ENST00000638071.1:c.1598G>T
|
|
|
ENST00000640639.1:c.1140G>T
|
ENSP00000491823.1:p.Gln380His
|
|
ENST00000371394.6:c.*1706G>T
|
ENSP00000485945.1:n.*1706G>T
|
|
ENST00000460843.5:c.1971G>T
|
ENSP00000417980.1:p.Gln657His
|
|
ENST00000462484.5:c.1971G>T
|
ENSP00000417328.1:p.Gln657His
|
|
ENST00000462942.3:c.828G>T
|
ENSP00000436107.1:p.Gln276His
|
|
ENST00000626603.1:n.1652C>A
|
|
|
NM_001145527.1:c.1971G>T
|
NP_001138999.1:p.Gln657His
|
|
NM_024757.4:c.1971G>T
|
NP_079033.4:p.Gln657His
|
|
XM_005266105.3:c.1962G>T
|
XP_005266162.1:p.Gln654His
|
|
XM_005266110.1:c.1878G>T
|
XP_005266167.1:p.Gln626His
|
|
XM_006717288.2:c.1953G>T
|
XP_006717351.1:p.Gln651His
|
|
XM_011519021.1:c.1980G>T
|
XP_011517323.1:p.Gln660His
|
|
XM_011519022.1:c.1977G>T
|
XP_011517324.1:p.Gln659His
|
|
XM_011519023.1:c.1959G>T
|
XP_011517325.1:p.Gln653His
|
|
XM_011519024.1:c.1902G>T
|
XP_011517326.1:p.Gln634His
|
|
XM_011519025.1:c.1878G>T
|
XP_011517327.1:p.Gln626His
|
|
XM_011519026.1:c.1836G>T
|
XP_011517328.1:p.Gln612His
|
|
XM_011519027.1:c.1980G>T
|
XP_011517329.1:p.Gln660His
|
|
XM_011519028.1:c.1980G>T
|
XP_011517330.1:p.Gln660His
|
|
XM_011519029.1:c.402G>T
|
XP_011517331.1:p.Gln134His
|
|
XM_011519033.1:c.1815G>T
|
XP_011517335.1:p.Gln605His
|
|
NM_001354259.1:c.1878G>T
|
NP_001341188.1:p.Gln626His
|
|
NM_001354263.1:c.1950G>T
|
NP_001341192.1:p.Gln650His
|
|
XM_005266105.5:c.1962G>T
|
XP_005266162.1:p.Gln654His
|
|
XM_011519021.3:c.1980G>T
|
XP_011517323.1:p.Gln660His
|
|
XM_011519022.3:c.1977G>T
|
XP_011517324.1:p.Gln659His
|
|
XM_011519023.3:c.1959G>T
|
XP_011517325.1:p.Gln653His
|
|
XM_011519029.3:c.402G>T
|
XP_011517331.1:p.Gln134His
|
|
XM_017015134.1:c.1956G>T
|
XP_016870623.1:p.Gln652His
|
|
XM_017015136.2:c.1872G>T
|
XP_016870625.1:p.Gln624His
|
|
XM_017015137.1:c.1857G>T
|
XP_016870626.1:p.Gln619His
|
|
XM_017015138.1:c.1857G>T
|
XP_016870627.1:p.Gln619His
|
|
XM_024447674.1:c.1800G>T
|
XP_024303442.1:p.Gln600His
|
|
XM_024447675.1:c.1734G>T
|
XP_024303443.1:p.Gln578His
|
|
XM_024447676.1:c.1095G>T
|
XP_024303444.1:p.Gln365His
|
|
XM_024447677.1:c.1095G>T
|
XP_024303445.1:p.Gln365His
|
|
XM_024447678.1:c.1878G>T
|
XP_024303446.1:p.Gln626His
|
|
XM_024447679.1:c.1878G>T
|
XP_024303447.1:p.Gln626His
|
|
XM_024447680.1:c.1713G>T
|
XP_024303448.1:p.Gln571His
|
|
NM_024757.5:c.1971G>T
MANE Select
|
NP_079033.4:p.Gln657His
|
|
NM_001145527.2:c.1971G>T
|
NP_001138999.1:p.Gln657His
|
|
NM_001354259.2:c.1878G>T
|
NP_001341188.1:p.Gln626His
|
|
NM_001354263.2:c.1950G>T
|
NP_001341192.1:p.Gln650His
|
|