ENST00000398636.8:c.56T>C
MANE Select
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ENSP00000381633.3:p.Val19Ala
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ENST00000398636.7:c.56T>C
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ENSP00000381633.3:p.Val19Ala
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ENST00000419470.6:c.101T>C
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ENSP00000397082.2:p.Val34Ala
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ENST00000428376.6:c.56T>C
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ENSP00000411102.2:p.Val19Ala
|
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ENST00000429958.5:c.56T>C
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ENSP00000395527.1:p.Val19Ala
|
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ENST00000439264.1:c.56T>C
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ENSP00000401649.1:p.Val19Ala
|
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ENST00000486922.1:n.325T>C
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|
|
NM_001093770.2:c.101T>C
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NP_001087239.2:p.Val34Ala
|
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NM_001164644.1:c.56T>C
|
NP_001158116.1:p.Val19Ala
|
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NM_001164645.1:c.101T>C
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NP_001158117.1:p.Val34Ala
|
|
NM_001164646.1:c.56T>C
|
NP_001158118.1:p.Val19Ala
|
|
NM_001164647.1:c.56T>C
|
NP_001158119.1:p.Val19Ala
|
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NM_005411.4:c.56T>C
|
NP_005402.3:p.Val19Ala
|
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XM_005270062.3:c.56T>C
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XP_005270119.1:p.Val19Ala
|
|
XM_006717953.2:c.101T>C
|
XP_006718016.1:p.Val34Ala
|
|
XM_005270062.5:c.56T>C
|
XP_005270119.1:p.Val19Ala
|
|
NM_001093770.3:c.101T>C
|
NP_001087239.2:p.Val34Ala
|
|
NM_001164644.2:c.56T>C
|
NP_001158116.1:p.Val19Ala
|
|
NM_001164645.2:c.101T>C
|
NP_001158117.1:p.Val34Ala
|
|
NM_001164646.2:c.56T>C
|
NP_001158118.1:p.Val19Ala
|
|
NM_005411.5:c.56T>C
MANE Select
|
NP_005402.3:p.Val19Ala
|
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