ENST00000532043.2:n.231T>A
|
|
|
ENST00000682266.1:c.1764T>A
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ENSP00000507766.1:p.Ala588=
|
|
ENST00000682341.1:c.2172T>A
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ENSP00000508251.1:p.Ala724=
|
|
ENST00000683197.1:c.2172T>A
|
ENSP00000507641.1:p.Ala724=
|
|
ENST00000683411.1:c.1764T>A
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ENSP00000508397.1:p.Ala588=
|
|
ENST00000683437.1:c.1764T>A
|
ENSP00000508408.1:p.Ala588=
|
|
ENST00000683613.1:n.3208T>A
|
|
|
ENST00000684663.1:c.2169T>A
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ENSP00000508009.1:p.Ala723=
|
|
ENST00000324559.9:c.2214T>A
MANE Select
|
ENSP00000315371.9:p.Ala738=
|
|
ENST00000648804.1:n.2549T>A
|
|
|
ENST00000324559.8:c.2214T>A
|
ENSP00000315371.8:p.Ala738=
|
|
ENST00000532043.1:n.231T>A
|
|
|
NM_001142649.1:c.2211T>A
|
NP_001136121.1:p.Ala737=
|
|
NM_213599.2:c.2214T>A , LRG_868t1:c.2214T>A
|
NP_998764.1:p.Ala738=
|
|
XM_005252820.2:c.2172T>A
|
XP_005252877.2:p.Ala724=
|
|
XM_005252821.2:c.2169T>A
|
XP_005252878.2:p.Ala723=
|
|
XM_005252822.3:c.2136T>A
|
XP_005252879.1:p.Ala712=
|
|
XM_005252823.3:c.2133T>A
|
XP_005252880.1:p.Ala711=
|
|
XM_011519949.1:c.2121T>A
|
XP_011518251.1:p.Ala707=
|
|
XM_005252820.3:c.2172T>A
|
XP_005252877.2:p.Ala724=
|
|
XM_005252821.3:c.2169T>A
|
XP_005252878.2:p.Ala723=
|
|
XM_005252822.4:c.2136T>A
|
XP_005252879.1:p.Ala712=
|
|
XM_011519949.2:c.2121T>A
|
XP_011518251.1:p.Ala707=
|
|
NM_001142649.2:c.2211T>A
|
NP_001136121.1:p.Ala737=
|
|
NM_213599.3:c.2214T>A
MANE Select
|
NP_998764.1:p.Ala738=
|
|