|
ENST00000251038.10:c.2167C>G
MANE Select
|
ENSP00000251038.5:p.Pro723Ala
|
|
|
ENST00000649731.1:c.*1375C>G
|
ENSP00000497757.1:n.*1375C>G
|
|
|
ENST00000251038.9:c.2167C>G
|
ENSP00000251038.5:p.Pro723Ala
|
|
|
ENST00000302216.12:c.1696C>G
|
ENSP00000307025.8:p.Pro566Ala
|
|
|
ENST00000318308.10:c.877C>G
|
ENSP00000327176.6:p.Pro293Ala
|
|
|
ENST00000336693.8:c.1672C>G
|
ENSP00000338002.4:p.Pro558Ala
|
|
|
ENST00000393514.9:c.2092C>G
|
ENSP00000377150.5:p.Pro698Ala
|
|
|
ENST00000406216.7:c.805C>G
|
ENSP00000384682.3:p.Pro269Ala
|
|
|
ENST00000554020.5:n.1010C>G
|
|
|
|
ENST00000555755.5:c.2149C>G
|
ENSP00000452475.1:p.Pro717Ala
|
|
|
ENST00000555792.1:c.412C>G
|
ENSP00000450823.1:p.Pro138Ala
|
|
|
ENST00000555851.6:n.326C>G
|
|
|
|
ENST00000555900.5:c.1273C>G
|
ENSP00000451530.1:p.Pro425Ala
|
|
|
ENST00000556000.5:c.1911C>G
|
|
|
|
ENST00000556945.5:c.1774C>G
|
ENSP00000450474.1:p.Pro592Ala
|
|
|
ENST00000557491.1:n.1452C>G
|
|
|
|
ENST00000557607.5:c.1219C>G
|
ENSP00000452370.1:p.Pro407Ala
|
|
|
NM_001160103.1:c.2164C>G
|
NP_001153575.1:p.Pro722Ala
|
|
|
NM_001160104.1:c.2149C>G
|
NP_001153576.1:p.Pro717Ala
|
|
|
NM_024824.4:c.2167C>G
|
NP_079100.2:p.Pro723Ala
|
|
|
NM_207660.3:c.1696C>G
|
NP_997543.1:p.Pro566Ala
|
|
|
NM_207661.2:c.1672C>G
|
NP_997544.1:p.Pro558Ala
|
|
|
NM_207662.3:c.877C>G
|
NP_997545.2:p.Pro293Ala
|
|
|
XM_005268067.3:c.2152C>G
|
XP_005268124.1:p.Pro718Ala
|
|
|
XM_005268068.3:c.2092C>G
|
XP_005268125.1:p.Pro698Ala
|
|
|
XM_005268069.3:c.1774C>G
|
XP_005268126.1:p.Pro592Ala
|
|
|
XM_005268070.3:c.1771C>G
|
XP_005268127.1:p.Pro591Ala
|
|
|
XM_005268071.3:c.1699C>G
|
XP_005268128.1:p.Pro567Ala
|
|
|
XM_005268073.3:c.1273C>G
|
XP_005268130.1:p.Pro425Ala
|
|
|
XM_006720257.2:c.1198C>G
|
XP_006720320.1:p.Pro400Ala
|
|
|
XM_011537160.1:c.2065C>G
|
XP_011535462.1:p.Pro689Ala
|
|
|
XM_011537161.1:c.2011C>G
|
XP_011535463.1:p.Pro671Ala
|
|
|
NM_001326295.1:c.1774C>G
|
NP_001313224.1:p.Pro592Ala
|
|
|
NM_001326296.1:c.2089C>G
|
NP_001313225.1:p.Pro697Ala
|
|
|
NM_001326297.1:c.2065C>G
|
NP_001313226.1:p.Pro689Ala
|
|
|
NM_001326298.1:c.1699C>G
|
NP_001313227.1:p.Pro567Ala
|
|
|
NM_001326299.1:c.2074C>G
|
NP_001313228.1:p.Pro692Ala
|
|
|
NM_001326300.1:c.1702C>G
|
NP_001313229.1:p.Pro568Ala
|
|
|
NM_001326301.1:c.1990C>G
|
NP_001313230.1:p.Pro664Ala
|
|
|
NM_001326302.1:c.1699C>G
|
NP_001313231.1:p.Pro567Ala
|
|
|
NM_001326303.1:c.1594C>G
|
NP_001313232.1:p.Pro532Ala
|
|
|
NM_001326304.1:c.1306C>G
|
NP_001313233.1:p.Pro436Ala
|
|
|
NM_001326305.1:c.1627C>G
|
NP_001313234.1:p.Pro543Ala
|
|
|
NM_001326306.1:c.1540C>G
|
NP_001313235.1:p.Pro514Ala
|
|
|
NM_001326307.1:c.2092C>G
|
NP_001313236.1:p.Pro698Ala
|
|
|
NM_001326308.1:c.1309C>G
|
NP_001313237.1:p.Pro437Ala
|
|
|
NM_001326309.1:c.1234C>G
|
NP_001313238.1:p.Pro412Ala
|
|
|
NM_001326310.1:c.2152C>G
|
NP_001313239.1:p.Pro718Ala
|
|
|
NM_001326311.1:c.1231C>G
|
NP_001313240.1:p.Pro411Ala
|
|
|
NM_001326312.1:c.2077C>G
|
NP_001313241.1:p.Pro693Ala
|
|
|
NM_001326313.1:c.1543C>G
|
NP_001313242.1:p.Pro515Ala
|
|
|
NM_001326314.1:c.1624C>G
|
NP_001313243.1:p.Pro542Ala
|
|
|
NM_001326315.1:c.2062C>G
|
NP_001313244.1:p.Pro688Ala
|
|
|
NM_001326316.1:c.2062C>G
|
NP_001313245.1:p.Pro688Ala
|
|
|
NR_136936.1:n.2232C>G
|
|
|
|
XM_005268070.5:c.1771C>G
|
XP_005268127.1:p.Pro591Ala
|
|
|
XM_005268073.4:c.1273C>G
|
XP_005268130.1:p.Pro425Ala
|
|
|
XM_006720257.3:c.1198C>G
|
XP_006720320.1:p.Pro400Ala
|
|
|
XM_011537161.3:c.2011C>G
|
XP_011535463.1:p.Pro671Ala
|
|
|
XM_024449713.1:c.1195C>G
|
XP_024305481.1:p.Pro399Ala
|
|
|
NM_024824.5:c.2167C>G
MANE Select
|
NP_079100.2:p.Pro723Ala
|
|
|
NM_001160103.2:c.2164C>G
|
NP_001153575.1:p.Pro722Ala
|
|
|
NM_001160104.2:c.2149C>G
|
NP_001153576.1:p.Pro717Ala
|
|
|
NM_001326295.2:c.1774C>G
|
NP_001313224.1:p.Pro592Ala
|
|
|
NM_001326296.2:c.2089C>G
|
NP_001313225.1:p.Pro697Ala
|
|
|
NM_001326297.2:c.2065C>G
|
NP_001313226.1:p.Pro689Ala
|
|
|
NM_001326298.2:c.1699C>G
|
NP_001313227.1:p.Pro567Ala
|
|
|
NM_001326299.2:c.2074C>G
|
NP_001313228.1:p.Pro692Ala
|
|
|
NM_001326300.2:c.1702C>G
|
NP_001313229.1:p.Pro568Ala
|
|
|
NM_001326301.2:c.1990C>G
|
NP_001313230.1:p.Pro664Ala
|
|
|
NM_001326302.2:c.1699C>G
|
NP_001313231.1:p.Pro567Ala
|
|
|
NM_001326303.2:c.1594C>G
|
NP_001313232.1:p.Pro532Ala
|
|
|
NM_001326304.2:c.1306C>G
|
NP_001313233.1:p.Pro436Ala
|
|
|
NM_001326305.2:c.1627C>G
|
NP_001313234.1:p.Pro543Ala
|
|
|
NM_001326306.2:c.1540C>G
|
NP_001313235.1:p.Pro514Ala
|
|
|
NM_001326307.2:c.2092C>G
|
NP_001313236.1:p.Pro698Ala
|
|
|
NM_001326308.2:c.1309C>G
|
NP_001313237.1:p.Pro437Ala
|
|
|
NM_001326309.2:c.1234C>G
|
NP_001313238.1:p.Pro412Ala
|
|
|
NM_001326310.2:c.2152C>G
|
NP_001313239.1:p.Pro718Ala
|
|
|
NM_001326311.2:c.1231C>G
|
NP_001313240.1:p.Pro411Ala
|
|
|
NM_001326312.2:c.2077C>G
|
NP_001313241.1:p.Pro693Ala
|
|
|
NM_001326313.2:c.1543C>G
|
NP_001313242.1:p.Pro515Ala
|
|
|
NM_001326314.2:c.1624C>G
|
NP_001313243.1:p.Pro542Ala
|
|
|
NM_001326315.2:c.2062C>G
|
NP_001313244.1:p.Pro688Ala
|
|
|
NM_207660.4:c.1696C>G
|
NP_997543.1:p.Pro566Ala
|
|
|
NM_207662.4:c.877C>G
|
NP_997545.2:p.Pro293Ala
|
|
|
NR_136936.2:n.2104C>G
|
|
|
|
NM_001326316.2:c.2062C>G
|
NP_001313245.1:p.Pro688Ala
|
|
|
NM_207661.3:c.1672C>G
|
NP_997544.1:p.Pro558Ala
|
|
