ENST00000578493.2:n.935C=
|
|
|
ENST00000699291.1:c.727C=
|
ENSP00000514272.1:n.727C=
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|
ENST00000699292.1:n.642C=
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|
|
ENST00000225275.4:c.1602C=
MANE Select
|
ENSP00000225275.3:p.Ser534=
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|
ENST00000225275.3:c.1602C=
|
ENSP00000225275.3:p.Ser534=
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|
ENST00000577220.1:c.60C=
|
ENSP00000464668.1:p.Ser20=
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|
NM_000250.1:c.1602C= , LRG_84t1:c.1602C=
|
NP_000241.1:p.Ser534=
|
|
XM_011524821.1:c.1788C=
|
XP_011523123.1:p.Ser596=
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|
XM_011524822.1:c.1317C=
|
XP_011523124.1:p.Ser439=
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|
XM_011524823.1:c.*151C=
|
XP_011523125.1:n.*151C=
|
|
NM_000250.2:c.1602C=
MANE Select
|
NP_000241.1:p.Ser534=
|
|