ENST00000409709.9:c.6217T>G
MANE Select
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ENSP00000386331.3:p.Ser2073Ala
|
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ENST00000670577.1:c.4018T>G
|
|
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ENST00000409619.6:c.6070T>G
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ENSP00000386635.2:p.Ser2024Ala
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ENST00000409709.7:c.6217T>G
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ENSP00000386331.3:p.Ser2073Ala
|
|
ENST00000458169.2:c.3643T>G
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ENSP00000417017.2:p.Ser1215Ala
|
|
ENST00000458637.6:c.6103T>G
|
ENSP00000392185.2:p.Ser2035Ala
|
|
ENST00000481328.7:n.3753T>G
|
|
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ENST00000526863.2:n.25+406T>G
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|
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ENST00000605744.1:n.1684T>G
|
|
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NM_000260.3:c.6217T>G
|
NP_000251.3:p.Ser2073Ala
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NM_001127180.1:c.6103T>G
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NP_001120652.1:p.Ser2035Ala
|
|
XM_005274012.2:c.6100T>G
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XP_005274069.1:p.Ser2034Ala
|
|
XM_006718558.2:c.6208T>G
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XP_006718621.1:p.Ser2070Ala
|
|
XM_006718559.2:c.6103T>G
|
XP_006718622.1:p.Ser2035Ala
|
|
XM_006718560.2:c.6100T>G
|
XP_006718623.1:p.Ser2034Ala
|
|
XM_006718561.2:c.6103T>G
|
XP_006718624.1:p.Ser2035Ala
|
|
XM_011545044.1:c.6217T>G
|
XP_011543346.1:p.Ser2073Ala
|
|
XM_011545045.1:c.6211T>G
|
XP_011543347.1:p.Ser2071Ala
|
|
XM_011545046.1:c.6184T>G
|
XP_011543348.1:p.Ser2062Ala
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|
XM_011545047.1:c.6121T>G
|
XP_011543349.1:p.Ser2041Ala
|
|
XM_011545048.1:c.5992T>G
|
XP_011543350.1:p.Ser1998Ala
|
|
XM_011545049.1:c.5980T>G
|
XP_011543351.1:p.Ser1994Ala
|
|
XM_011545050.1:c.5953T>G
|
XP_011543352.1:p.Ser1985Ala
|
|
XM_011545051.1:c.6217T>G
|
XP_011543353.1:p.Ser2073Ala
|
|
XR_949938.1:n.6537T>G
|
|
|
XR_949941.1:n.6511T>G
|
|
|
XM_011545044.2:c.6217T>G
|
XP_011543346.1:p.Ser2073Ala
|
|
XM_011545046.2:c.6307T>G
|
XP_011543348.2:p.Ser2103Ala
|
|
XM_011545050.2:c.5953T>G
|
XP_011543352.1:p.Ser1985Ala
|
|
XM_017017778.1:c.6301T>G
|
XP_016873267.1:p.Ser2101Ala
|
|
XM_017017779.1:c.6298T>G
|
XP_016873268.1:p.Ser2100Ala
|
|
XM_017017780.1:c.6307T>G
|
XP_016873269.1:p.Ser2103Ala
|
|
XM_017017781.1:c.6211T>G
|
XP_016873270.1:p.Ser2071Ala
|
|
XM_017017782.1:c.6193T>G
|
XP_016873271.1:p.Ser2065Ala
|
|
XM_017017783.1:c.6190T>G
|
XP_016873272.1:p.Ser2064Ala
|
|
XM_017017784.1:c.6190T>G
|
XP_016873273.1:p.Ser2064Ala
|
|
XM_017017785.1:c.6070T>G
|
XP_016873274.1:p.Ser2024Ala
|
|
XM_017017786.1:c.6307T>G
|
XP_016873275.1:p.Ser2103Ala
|
|
XM_017017788.1:c.6193T>G
|
XP_016873277.1:p.Ser2065Ala
|
|
XR_001747885.1:n.6296T>G
|
|
|
XR_001747887.1:n.6282T>G
|
|
|
NM_000260.4:c.6217T>G
MANE Select
|
NP_000251.3:p.Ser2073Ala
|
|
NM_001127180.2:c.6103T>G
|
NP_001120652.1:p.Ser2035Ala
|
|
NM_001369365.1:c.6070T>G
|
NP_001356294.1:p.Ser2024Ala
|
|