ENST00000369244.7:c.1820A=
MANE Select
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ENSP00000358247.1:p.Asn607=
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|
ENST00000229971.2:c.1820A=
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ENSP00000229971.1:p.Asn607=
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|
ENST00000369244.6:c.1820A=
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ENSP00000358247.1:p.Asn607=
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NM_001278716.1:c.1820A=
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NP_001265645.1:p.Asn607=
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NM_012160.4:c.1820A=
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NP_036292.2:p.Asn607=
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NR_103836.1:n.1865A=
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|
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XM_005266930.1:c.1748A=
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XP_005266987.1:p.Asn583=
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|
XM_005266930.3:c.1748A=
|
XP_005266987.1:p.Asn583=
|
|
XM_017010726.1:c.1820A=
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XP_016866215.1:p.Asn607=
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|
XM_017010727.2:c.1748A=
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XP_016866216.1:p.Asn583=
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|
XM_017010728.1:c.1094A=
|
XP_016866217.1:p.Asn365=
|
|
NM_001278716.2:c.1820A=
MANE Select
|
NP_001265645.1:p.Asn607=
|
|
NR_103836.2:n.1805A=
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|
|
NM_012160.5:c.1820A=
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NP_036292.2:p.Asn607=
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