ENST00000234071.8:c.678G=
MANE Select
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ENSP00000234071.4:p.Gln226=
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ENST00000234071.7:c.678G=
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ENSP00000234071.3:p.Gln226=
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|
ENST00000402125.2:c.121-2130G=
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|
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ENST00000409048.1:c.780G=
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ENSP00000386679.1:p.Gln260=
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|
ENST00000464089.1:n.264G=
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|
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NM_000312.3:c.678G= , LRG_599t1:c.678G=
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NP_000303.1:p.Gln226=
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|
XM_005263715.3:c.861G=
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XP_005263772.1:p.Gln287=
|
|
XM_005263716.3:c.843G=
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XP_005263773.1:p.Gln281=
|
|
XM_005263717.3:c.741G=
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XP_005263774.1:p.Gln247=
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|
XM_005263717.4:c.741G=
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XP_005263774.1:p.Gln247=
|
|
XM_017004505.1:c.921G=
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XP_016859994.1:p.Gln307=
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|
XM_024453002.1:c.1023G=
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XP_024308770.1:p.Gln341=
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|
XM_024453003.1:c.963G=
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XP_024308771.1:p.Gln321=
|
|
XM_024453004.1:c.861G=
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XP_024308772.1:p.Gln287=
|
|
XM_024453005.1:c.843G=
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XP_024308773.1:p.Gln281=
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|
XM_024453006.1:c.780G=
|
XP_024308774.1:p.Gln260=
|
|
XR_923313.2:n.4358C=
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|
|
NM_000312.4:c.678G=
MANE Select
|
NP_000303.1:p.Gln226=
|
|
NM_001375602.1:c.861G=
|
NP_001362531.1:p.Gln287=
|
|
NM_001375603.1:c.843G=
|
NP_001362532.1:p.Gln281=
|
|
NM_001375604.1:c.741G=
|
NP_001362533.1:p.Gln247=
|
|
NM_001375605.1:c.780G=
|
NP_001362534.1:p.Gln260=
|
|
NM_001375606.1:c.846G=
|
NP_001362535.1:p.Gln282=
|
|
NM_001375607.1:c.864G=
|
NP_001362536.1:p.Gln288=
|
|
NM_001375608.1:c.621G=
|
NP_001362537.1:p.Gln207=
|
|
NM_001375609.1:c.654G=
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NP_001362538.1:p.Gln218=
|
|
NM_001375610.1:c.672G=
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NP_001362539.1:p.Gln224=
|
|
NM_001375611.1:c.678G=
|
NP_001362540.1:p.Gln226=
|
|
NM_001375613.1:c.678G=
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NP_001362542.1:p.Gln226=
|
|