|
ENST00000251038.10:c.2173C>G
MANE Select
|
ENSP00000251038.5:p.His725Asp
|
|
|
ENST00000649731.1:c.*1381C>G
|
ENSP00000497757.1:n.*1381C>G
|
|
|
ENST00000251038.9:c.2173C>G
|
ENSP00000251038.5:p.His725Asp
|
|
|
ENST00000302216.12:c.1702C>G
|
ENSP00000307025.8:p.His568Asp
|
|
|
ENST00000318308.10:c.883C>G
|
ENSP00000327176.6:p.His295Asp
|
|
|
ENST00000336693.8:c.1678C>G
|
ENSP00000338002.4:p.His560Asp
|
|
|
ENST00000393514.9:c.2098C>G
|
ENSP00000377150.5:p.His700Asp
|
|
|
ENST00000406216.7:c.811C>G
|
ENSP00000384682.3:p.His271Asp
|
|
|
ENST00000554020.5:n.1016C>G
|
|
|
|
ENST00000555755.5:c.2155C>G
|
ENSP00000452475.1:p.His719Asp
|
|
|
ENST00000555792.1:c.418C>G
|
ENSP00000450823.1:p.His140Asp
|
|
|
ENST00000555851.6:n.332C>G
|
|
|
|
ENST00000555900.5:c.1279C>G
|
ENSP00000451530.1:p.His427Asp
|
|
|
ENST00000556000.5:c.1917C>G
|
|
|
|
ENST00000556945.5:c.1780C>G
|
ENSP00000450474.1:p.His594Asp
|
|
|
ENST00000557491.1:n.1458C>G
|
|
|
|
ENST00000557607.5:c.1225C>G
|
ENSP00000452370.1:p.His409Asp
|
|
|
NM_001160103.1:c.2170C>G
|
NP_001153575.1:p.His724Asp
|
|
|
NM_001160104.1:c.2155C>G
|
NP_001153576.1:p.His719Asp
|
|
|
NM_024824.4:c.2173C>G
|
NP_079100.2:p.His725Asp
|
|
|
NM_207660.3:c.1702C>G
|
NP_997543.1:p.His568Asp
|
|
|
NM_207661.2:c.1678C>G
|
NP_997544.1:p.His560Asp
|
|
|
NM_207662.3:c.883C>G
|
NP_997545.2:p.His295Asp
|
|
|
XM_005268067.3:c.2158C>G
|
XP_005268124.1:p.His720Asp
|
|
|
XM_005268068.3:c.2098C>G
|
XP_005268125.1:p.His700Asp
|
|
|
XM_005268069.3:c.1780C>G
|
XP_005268126.1:p.His594Asp
|
|
|
XM_005268070.3:c.1777C>G
|
XP_005268127.1:p.His593Asp
|
|
|
XM_005268071.3:c.1705C>G
|
XP_005268128.1:p.His569Asp
|
|
|
XM_005268073.3:c.1279C>G
|
XP_005268130.1:p.His427Asp
|
|
|
XM_006720257.2:c.1204C>G
|
XP_006720320.1:p.His402Asp
|
|
|
XM_011537160.1:c.2071C>G
|
XP_011535462.1:p.His691Asp
|
|
|
XM_011537161.1:c.2017C>G
|
XP_011535463.1:p.His673Asp
|
|
|
NM_001326295.1:c.1780C>G
|
NP_001313224.1:p.His594Asp
|
|
|
NM_001326296.1:c.2095C>G
|
NP_001313225.1:p.His699Asp
|
|
|
NM_001326297.1:c.2071C>G
|
NP_001313226.1:p.His691Asp
|
|
|
NM_001326298.1:c.1705C>G
|
NP_001313227.1:p.His569Asp
|
|
|
NM_001326299.1:c.2080C>G
|
NP_001313228.1:p.His694Asp
|
|
|
NM_001326300.1:c.1708C>G
|
NP_001313229.1:p.His570Asp
|
|
|
NM_001326301.1:c.1996C>G
|
NP_001313230.1:p.His666Asp
|
|
|
NM_001326302.1:c.1705C>G
|
NP_001313231.1:p.His569Asp
|
|
|
NM_001326303.1:c.1600C>G
|
NP_001313232.1:p.His534Asp
|
|
|
NM_001326304.1:c.1312C>G
|
NP_001313233.1:p.His438Asp
|
|
|
NM_001326305.1:c.1633C>G
|
NP_001313234.1:p.His545Asp
|
|
|
NM_001326306.1:c.1546C>G
|
NP_001313235.1:p.His516Asp
|
|
|
NM_001326307.1:c.2098C>G
|
NP_001313236.1:p.His700Asp
|
|
|
NM_001326308.1:c.1315C>G
|
NP_001313237.1:p.His439Asp
|
|
|
NM_001326309.1:c.1240C>G
|
NP_001313238.1:p.His414Asp
|
|
|
NM_001326310.1:c.2158C>G
|
NP_001313239.1:p.His720Asp
|
|
|
NM_001326311.1:c.1237C>G
|
NP_001313240.1:p.His413Asp
|
|
|
NM_001326312.1:c.2083C>G
|
NP_001313241.1:p.His695Asp
|
|
|
NM_001326313.1:c.1549C>G
|
NP_001313242.1:p.His517Asp
|
|
|
NM_001326314.1:c.1630C>G
|
NP_001313243.1:p.His544Asp
|
|
|
NM_001326315.1:c.2068C>G
|
NP_001313244.1:p.His690Asp
|
|
|
NM_001326316.1:c.2068C>G
|
NP_001313245.1:p.His690Asp
|
|
|
NR_136936.1:n.2238C>G
|
|
|
|
XM_005268070.5:c.1777C>G
|
XP_005268127.1:p.His593Asp
|
|
|
XM_005268073.4:c.1279C>G
|
XP_005268130.1:p.His427Asp
|
|
|
XM_006720257.3:c.1204C>G
|
XP_006720320.1:p.His402Asp
|
|
|
XM_011537161.3:c.2017C>G
|
XP_011535463.1:p.His673Asp
|
|
|
XM_024449713.1:c.1201C>G
|
XP_024305481.1:p.His401Asp
|
|
|
NM_024824.5:c.2173C>G
MANE Select
|
NP_079100.2:p.His725Asp
|
|
|
NM_001160103.2:c.2170C>G
|
NP_001153575.1:p.His724Asp
|
|
|
NM_001160104.2:c.2155C>G
|
NP_001153576.1:p.His719Asp
|
|
|
NM_001326295.2:c.1780C>G
|
NP_001313224.1:p.His594Asp
|
|
|
NM_001326296.2:c.2095C>G
|
NP_001313225.1:p.His699Asp
|
|
|
NM_001326297.2:c.2071C>G
|
NP_001313226.1:p.His691Asp
|
|
|
NM_001326298.2:c.1705C>G
|
NP_001313227.1:p.His569Asp
|
|
|
NM_001326299.2:c.2080C>G
|
NP_001313228.1:p.His694Asp
|
|
|
NM_001326300.2:c.1708C>G
|
NP_001313229.1:p.His570Asp
|
|
|
NM_001326301.2:c.1996C>G
|
NP_001313230.1:p.His666Asp
|
|
|
NM_001326302.2:c.1705C>G
|
NP_001313231.1:p.His569Asp
|
|
|
NM_001326303.2:c.1600C>G
|
NP_001313232.1:p.His534Asp
|
|
|
NM_001326304.2:c.1312C>G
|
NP_001313233.1:p.His438Asp
|
|
|
NM_001326305.2:c.1633C>G
|
NP_001313234.1:p.His545Asp
|
|
|
NM_001326306.2:c.1546C>G
|
NP_001313235.1:p.His516Asp
|
|
|
NM_001326307.2:c.2098C>G
|
NP_001313236.1:p.His700Asp
|
|
|
NM_001326308.2:c.1315C>G
|
NP_001313237.1:p.His439Asp
|
|
|
NM_001326309.2:c.1240C>G
|
NP_001313238.1:p.His414Asp
|
|
|
NM_001326310.2:c.2158C>G
|
NP_001313239.1:p.His720Asp
|
|
|
NM_001326311.2:c.1237C>G
|
NP_001313240.1:p.His413Asp
|
|
|
NM_001326312.2:c.2083C>G
|
NP_001313241.1:p.His695Asp
|
|
|
NM_001326313.2:c.1549C>G
|
NP_001313242.1:p.His517Asp
|
|
|
NM_001326314.2:c.1630C>G
|
NP_001313243.1:p.His544Asp
|
|
|
NM_001326315.2:c.2068C>G
|
NP_001313244.1:p.His690Asp
|
|
|
NM_207660.4:c.1702C>G
|
NP_997543.1:p.His568Asp
|
|
|
NM_207662.4:c.883C>G
|
NP_997545.2:p.His295Asp
|
|
|
NR_136936.2:n.2110C>G
|
|
|
|
NM_001326316.2:c.2068C>G
|
NP_001313245.1:p.His690Asp
|
|
|
NM_207661.3:c.1678C>G
|
NP_997544.1:p.His560Asp
|
|
