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ENST00000340611.9:c.1420A>G
MANE Select
|
ENSP00000339637.4:p.Thr474Ala
|
|
|
ENST00000340611.8:c.1420A>G
|
ENSP00000339637.4:p.Thr474Ala
|
|
|
ENST00000467558.5:n.2792A>G
|
|
|
|
ENST00000469750.5:n.3992A>G
|
|
|
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ENST00000473879.1:n.136A>G
|
|
|
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ENST00000493232.5:n.4156A>G
|
|
|
|
NM_152743.3:c.1420A>G
|
NP_689956.2:p.Thr474Ala
|
|
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XM_005249643.3:c.1420A>G
|
XP_005249700.1:p.Thr474Ala
|
|
|
XM_011515177.1:c.1504A>G
|
XP_011513479.1:p.Thr502Ala
|
|
|
XM_011515178.1:c.1504A>G
|
XP_011513480.1:p.Thr502Ala
|
|
|
XM_011515179.1:c.1501A>G
|
XP_011513481.1:p.Thr501Ala
|
|
|
XM_011515180.1:c.1474A>G
|
XP_011513482.1:p.Thr492Ala
|
|
|
XM_011515181.1:c.1504A>G
|
XP_011513483.1:p.Thr502Ala
|
|
|
XM_011515182.1:c.1504A>G
|
XP_011513484.1:p.Thr502Ala
|
|
|
XM_011515183.1:c.979A>G
|
XP_011513485.1:p.Thr327Ala
|
|
|
XM_011515184.1:c.979A>G
|
XP_011513486.1:p.Thr327Ala
|
|
|
XM_011515185.1:c.1420A>G
|
XP_011513487.1:p.Thr474Ala
|
|
|
XM_011515186.1:c.1504A>G
|
XP_011513488.1:p.Thr502Ala
|
|
|
XM_011515187.1:c.76A>G
|
XP_011513489.1:p.Thr26Ala
|
|
|
NM_001350626.1:c.1420A>G
|
NP_001337555.1:p.Thr474Ala
|
|
|
NM_001350627.1:c.895A>G
|
NP_001337556.1:p.Thr299Ala
|
|
|
NR_146879.1:n.1837A>G
|
|
|
|
XM_011515177.2:c.1504A>G
|
XP_011513479.1:p.Thr502Ala
|
|
|
XM_011515179.2:c.1501A>G
|
XP_011513481.1:p.Thr501Ala
|
|
|
XM_011515181.2:c.1504A>G
|
XP_011513483.1:p.Thr502Ala
|
|
|
XM_011515182.2:c.1504A>G
|
XP_011513484.1:p.Thr502Ala
|
|
|
XM_011515184.3:c.979A>G
|
XP_011513486.1:p.Thr327Ala
|
|
|
XM_011515186.2:c.1504A>G
|
XP_011513488.1:p.Thr502Ala
|
|
|
XM_017011833.1:c.1417A>G
|
XP_016867322.1:p.Thr473Ala
|
|
|
XM_017011834.1:c.1417A>G
|
XP_016867323.1:p.Thr473Ala
|
|
|
XM_017011836.2:c.1420A>G
|
XP_016867325.1:p.Thr474Ala
|
|
|
XM_024446682.1:c.76A>G
|
XP_024302450.1:p.Thr26Ala
|
|
|
NM_152743.4:c.1420A>G
MANE Select
|
NP_689956.2:p.Thr474Ala
|
|
|
NM_001350626.2:c.1420A>G
|
NP_001337555.1:p.Thr474Ala
|
|
|
NM_001350627.2:c.895A>G
|
NP_001337556.1:p.Thr299Ala
|
|
|
NR_146879.2:n.1603A>G
|
|
|
