ENST00000532043.2:n.189T>G
|
|
|
ENST00000682266.1:c.1722T>G
|
ENSP00000507766.1:p.Ala574=
|
|
ENST00000682341.1:c.2130T>G
|
ENSP00000508251.1:p.Ala710=
|
|
ENST00000683197.1:c.2130T>G
|
ENSP00000507641.1:p.Ala710=
|
|
ENST00000683411.1:c.1722T>G
|
ENSP00000508397.1:p.Ala574=
|
|
ENST00000683437.1:c.1722T>G
|
ENSP00000508408.1:p.Ala574=
|
|
ENST00000683613.1:n.3166T>G
|
|
|
ENST00000684663.1:c.2127T>G
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ENSP00000508009.1:p.Ala709=
|
|
ENST00000324559.9:c.2172T>G
MANE Select
|
ENSP00000315371.9:p.Ala724=
|
|
ENST00000648804.1:n.2507T>G
|
|
|
ENST00000324559.8:c.2172T>G
|
ENSP00000315371.8:p.Ala724=
|
|
ENST00000532043.1:n.189T>G
|
|
|
NM_001142649.1:c.2169T>G
|
NP_001136121.1:p.Ala723=
|
|
NM_213599.2:c.2172T>G , LRG_868t1:c.2172T>G
|
NP_998764.1:p.Ala724=
|
|
XM_005252820.2:c.2130T>G
|
XP_005252877.2:p.Ala710=
|
|
XM_005252821.2:c.2127T>G
|
XP_005252878.2:p.Ala709=
|
|
XM_005252822.3:c.2094T>G
|
XP_005252879.1:p.Ala698=
|
|
XM_005252823.3:c.2091T>G
|
XP_005252880.1:p.Ala697=
|
|
XM_011519949.1:c.2079T>G
|
XP_011518251.1:p.Ala693=
|
|
XM_005252820.3:c.2130T>G
|
XP_005252877.2:p.Ala710=
|
|
XM_005252821.3:c.2127T>G
|
XP_005252878.2:p.Ala709=
|
|
XM_005252822.4:c.2094T>G
|
XP_005252879.1:p.Ala698=
|
|
XM_011519949.2:c.2079T>G
|
XP_011518251.1:p.Ala693=
|
|
NM_001142649.2:c.2169T>G
|
NP_001136121.1:p.Ala723=
|
|
NM_213599.3:c.2172T>G
MANE Select
|
NP_998764.1:p.Ala724=
|
|