ENST00000262494.13:c.545C=
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ENSP00000262494.7:p.Thr182=
|
|
ENST00000262493.12:c.545C=
MANE Select
|
ENSP00000262493.6:p.Thr182=
|
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ENST00000262494.12:c.545C=
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ENSP00000262494.7:p.Thr182=
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|
ENST00000562316.6:c.212C=
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ENSP00000457238.2:p.Thr71=
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ENST00000638185.1:n.760C=
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|
|
ENST00000638210.1:n.845C=
|
|
|
ENST00000638705.1:c.545C=
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ENSP00000491223.1:p.Thr182=
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|
ENST00000638836.1:n.455C=
|
|
|
ENST00000639055.1:n.1266C=
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|
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ENST00000639251.1:n.446C=
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ENST00000639268.1:c.229-1922C=
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|
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ENST00000639341.1:c.70C=
|
|
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ENST00000639770.1:c.583C=
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ENSP00000491999.1:n.583C=
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|
ENST00000640390.1:n.475C=
|
|
|
ENST00000640893.1:c.384C=
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ENSP00000492677.1:p.Asn128=
|
|
ENST00000262493.10:c.545C=
|
ENSP00000262493.6:p.Thr182=
|
|
ENST00000262494.11:c.545C=
|
ENSP00000262494.7:p.Thr182=
|
|
ENST00000562316.5:c.284C=
|
ENSP00000457238.1:p.Thr95=
|
|
NM_020988.2:c.545C=
|
NP_066268.1:p.Thr182=
|
|
NM_138736.2:c.545C=
|
NP_620073.2:p.Thr182=
|
|
XM_011523003.1:c.419C=
|
XP_011521305.1:p.Thr140=
|
|
XM_011523003.3:c.419C=
|
XP_011521305.1:p.Thr140=
|
|
NM_020988.3:c.545C=
MANE Select
|
NP_066268.1:p.Thr182=
|
|
NM_138736.3:c.545C=
|
NP_620073.2:p.Thr182=
|
|