ENST00000234071.8:c.669C=
MANE Select
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ENSP00000234071.4:p.Ser223=
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ENST00000234071.7:c.669C=
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ENSP00000234071.3:p.Ser223=
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|
ENST00000402125.2:c.121-2139C=
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|
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ENST00000409048.1:c.771C=
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ENSP00000386679.1:p.Ser257=
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ENST00000464089.1:n.255C=
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|
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NM_000312.3:c.669C= , LRG_599t1:c.669C=
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NP_000303.1:p.Ser223=
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|
XM_005263715.3:c.852C=
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XP_005263772.1:p.Ser284=
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XM_005263716.3:c.834C=
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XP_005263773.1:p.Ser278=
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XM_005263717.3:c.732C=
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XP_005263774.1:p.Ser244=
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|
XM_005263717.4:c.732C=
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XP_005263774.1:p.Ser244=
|
|
XM_017004505.1:c.912C=
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XP_016859994.1:p.Ser304=
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|
XM_024453002.1:c.1014C=
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XP_024308770.1:p.Ser338=
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|
XM_024453003.1:c.954C=
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XP_024308771.1:p.Ser318=
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|
XM_024453004.1:c.852C=
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XP_024308772.1:p.Ser284=
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|
XM_024453005.1:c.834C=
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XP_024308773.1:p.Ser278=
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|
XM_024453006.1:c.771C=
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XP_024308774.1:p.Ser257=
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|
XR_923313.2:n.4367G=
|
|
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NM_000312.4:c.669C=
MANE Select
|
NP_000303.1:p.Ser223=
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|
NM_001375602.1:c.852C=
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NP_001362531.1:p.Ser284=
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|
NM_001375603.1:c.834C=
|
NP_001362532.1:p.Ser278=
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|
NM_001375604.1:c.732C=
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NP_001362533.1:p.Ser244=
|
|
NM_001375605.1:c.771C=
|
NP_001362534.1:p.Ser257=
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|
NM_001375606.1:c.837C=
|
NP_001362535.1:p.Ser279=
|
|
NM_001375607.1:c.855C=
|
NP_001362536.1:p.Ser285=
|
|
NM_001375608.1:c.612C=
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NP_001362537.1:p.Ser204=
|
|
NM_001375609.1:c.645C=
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NP_001362538.1:p.Ser215=
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|
NM_001375610.1:c.663C=
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NP_001362539.1:p.Ser221=
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|
NM_001375611.1:c.669C=
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NP_001362540.1:p.Ser223=
|
|
NM_001375613.1:c.669C=
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NP_001362542.1:p.Ser223=
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