ENST00000292408.9:c.571T>G
MANE Select
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ENSP00000292408.4:p.Phe191Val
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ENST00000292408.8:c.571T>G
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ENSP00000292408.4:p.Phe191Val
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ENST00000393637.5:c.571T>G
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ENSP00000377254.1:p.Phe191Val
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ENST00000393648.6:c.571T>G
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ENSP00000377259.2:p.Phe191Val
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ENST00000426612.5:n.688T>G
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|
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ENST00000430285.5:c.*435T>G
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ENSP00000395164.1:n.*435T>G
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ENST00000502906.5:c.571T>G
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ENSP00000424960.1:p.Phe191Val
|
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ENST00000503708.5:c.571T>G
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ENSP00000424905.1:p.Phe191Val
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ENST00000509511.5:n.571T>G
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|
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NM_001291980.1:c.571T>G
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NP_001278909.1:p.Phe191Val
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NM_002011.4:c.571T>G
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NP_002002.3:p.Phe191Val
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NM_022963.3:c.571T>G
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NP_075252.2:p.Phe191Val
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NM_213647.2:c.571T>G
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NP_998812.1:p.Phe191Val
|
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XM_005265838.2:c.571T>G
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XP_005265895.1:p.Phe191Val
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XM_011534464.1:c.664T>G
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XP_011532766.1:p.Phe222Val
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XM_011534465.1:c.253T>G
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XP_011532767.1:p.Phe85Val
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XR_941090.1:n.616T>G
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|
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NM_001354984.1:c.571T>G
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NP_001341913.1:p.Phe191Val
|
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NM_213647.3:c.571T>G
MANE Select
|
NP_998812.1:p.Phe191Val
|
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NM_001291980.2:c.571T>G
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NP_001278909.1:p.Phe191Val
|
|
NM_001354984.2:c.571T>G
|
NP_001341913.1:p.Phe191Val
|
|
NM_002011.5:c.571T>G
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NP_002002.3:p.Phe191Val
|
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