ENST00000578493.2:n.905T=
|
|
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ENST00000699291.1:c.697T=
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ENSP00000514272.1:n.697T=
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|
ENST00000699292.1:n.612T=
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|
|
ENST00000225275.4:c.1572T=
MANE Select
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ENSP00000225275.3:p.Arg524=
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|
ENST00000225275.3:c.1572T=
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ENSP00000225275.3:p.Arg524=
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ENST00000577220.1:c.30T=
|
ENSP00000464668.1:p.Arg10=
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|
NM_000250.1:c.1572T= , LRG_84t1:c.1572T=
|
NP_000241.1:p.Arg524=
|
|
XM_011524821.1:c.1758T=
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XP_011523123.1:p.Arg586=
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|
XM_011524822.1:c.1287T=
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XP_011523124.1:p.Arg429=
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|
XM_011524823.1:c.*121T=
|
XP_011523125.1:n.*121T=
|
|
NM_000250.2:c.1572T=
MANE Select
|
NP_000241.1:p.Arg524=
|
|