ENST00000426263.10:c.669G=
MANE Select
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ENSP00000416293.2:p.Arg223=
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|
ENST00000669445.1:c.46G=
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|
|
ENST00000674765.1:c.669G=
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ENSP00000501811.1:p.Arg223=
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|
ENST00000675112.1:n.692G=
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|
|
ENST00000676254.1:n.1118G=
|
|
|
ENST00000426263.7:c.669G=
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ENSP00000416293.2:p.Arg223=
|
|
ENST00000439722.2:c.548G=
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ENSP00000395521.2:n.548G=
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|
ENST00000475162.3:c.415+743G=
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|
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ENST00000630287.2:c.517-103G=
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ENSP00000486694.1:n.517-103G=
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|
NM_006516.2:c.669G=
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NP_006507.2:p.Arg223=
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|
NM_006516.3:c.669G=
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NP_006507.2:p.Arg223=
|
|
NM_006516.4:c.669G=
MANE Select
|
NP_006507.2:p.Arg223=
|
|