ENST00000378823.8:c.2696A=
MANE Select
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ENSP00000368100.4:p.Gln899=
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|
ENST00000638452.2:c.2399A=
|
ENSP00000492349.2:p.Gln800=
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|
ENST00000638504.1:n.2304A=
|
|
|
ENST00000638568.2:c.2399A=
|
ENSP00000491158.2:p.Gln800=
|
|
ENST00000639899.1:n.3215A=
|
|
|
ENST00000640655.2:c.2399A=
|
ENSP00000491596.2:p.Gln800=
|
|
ENST00000651160.1:c.*840A=
|
ENSP00000498829.1:n.*840A=
|
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ENST00000651723.1:c.*2779A=
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ENSP00000498237.1:n.*2779A=
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ENST00000652016.1:c.*913A=
|
ENSP00000498267.1:n.*913A=
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ENST00000378823.7:c.2696A=
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ENSP00000368100.4:p.Gln899=
|
|
ENST00000423956.5:c.*882A=
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ENSP00000390971.1:n.*882A=
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|
ENST00000533482.5:c.*2322A=
|
ENSP00000431225.1:n.*2322A=
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|
NM_005732.3:c.2696A=
|
NP_005723.2:p.Gln899=
|
|
NM_005732.4:c.2696A=
MANE Select
|
NP_005723.2:p.Gln899=
|
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