ENST00000234071.8:c.541T>G
MANE Select
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ENSP00000234071.4:p.Phe181Val
|
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ENST00000234071.7:c.541T>G
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ENSP00000234071.3:p.Phe181Val
|
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ENST00000402125.2:c.121-2267T>G
|
|
|
ENST00000409048.1:c.643T>G
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ENSP00000386679.1:p.Phe215Val
|
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ENST00000442644.5:c.484T>G
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ENSP00000411241.1:p.Phe162Val
|
|
ENST00000464089.1:n.127T>G
|
|
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NM_000312.3:c.541T>G , LRG_599t1:c.541T>G
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NP_000303.1:p.Phe181Val
|
|
XM_005263715.3:c.724T>G
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XP_005263772.1:p.Phe242Val
|
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XM_005263716.3:c.706T>G
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XP_005263773.1:p.Phe236Val
|
|
XM_005263717.3:c.604T>G
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XP_005263774.1:p.Phe202Val
|
|
XM_005263717.4:c.604T>G
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XP_005263774.1:p.Phe202Val
|
|
XM_017004505.1:c.784T>G
|
XP_016859994.1:p.Phe262Val
|
|
XM_024453002.1:c.886T>G
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XP_024308770.1:p.Phe296Val
|
|
XM_024453003.1:c.826T>G
|
XP_024308771.1:p.Phe276Val
|
|
XM_024453004.1:c.724T>G
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XP_024308772.1:p.Phe242Val
|
|
XM_024453005.1:c.706T>G
|
XP_024308773.1:p.Phe236Val
|
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XM_024453006.1:c.643T>G
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XP_024308774.1:p.Phe215Val
|
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XR_923313.2:n.4495A>C
|
|
|
NM_000312.4:c.541T>G
MANE Select
|
NP_000303.1:p.Phe181Val
|
|
NM_001375602.1:c.724T>G
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NP_001362531.1:p.Phe242Val
|
|
NM_001375603.1:c.706T>G
|
NP_001362532.1:p.Phe236Val
|
|
NM_001375604.1:c.604T>G
|
NP_001362533.1:p.Phe202Val
|
|
NM_001375605.1:c.643T>G
|
NP_001362534.1:p.Phe215Val
|
|
NM_001375606.1:c.709T>G
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NP_001362535.1:p.Phe237Val
|
|
NM_001375607.1:c.727T>G
|
NP_001362536.1:p.Phe243Val
|
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NM_001375608.1:c.484T>G
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NP_001362537.1:p.Phe162Val
|
|
NM_001375609.1:c.517T>G
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NP_001362538.1:p.Phe173Val
|
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NM_001375610.1:c.535T>G
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NP_001362539.1:p.Phe179Val
|
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NM_001375611.1:c.541T>G
|
NP_001362540.1:p.Phe181Val
|
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NM_001375613.1:c.541T>G
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NP_001362542.1:p.Phe181Val
|
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