ENST00000262493.12:c.987G=
MANE Select
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ENSP00000262493.6:p.Thr329=
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ENST00000562316.6:c.545-1128G=
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ENSP00000457238.2:n.545-1128G=
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ENST00000564727.2:c.291G=
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ENSP00000454971.2:p.Thr97=
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ENST00000568375.2:c.225G=
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ENST00000638210.1:n.1287G=
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|
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ENST00000638705.1:c.987G=
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ENSP00000491223.1:p.Thr329=
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ENST00000638836.1:n.897G=
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ENST00000639251.1:n.888G=
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ENST00000639268.1:c.622G=
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ENST00000639341.1:c.512G=
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ENST00000639770.1:c.1025G=
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ENSP00000491999.1:n.1025G=
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ENST00000640390.1:n.917G=
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|
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ENST00000640469.1:c.351G=
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ENSP00000491875.1:p.Thr117=
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ENST00000640560.1:n.763G=
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|
|
ENST00000640893.1:c.*385G=
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ENSP00000492677.1:n.*385G=
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ENST00000262493.10:c.987G=
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ENSP00000262493.6:p.Thr329=
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|
ENST00000564727.1:c.207G=
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ENSP00000454971.1:p.Thr69=
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|
ENST00000568375.1:n.225G=
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|
|
NM_020988.2:c.987G=
|
NP_066268.1:p.Thr329=
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|
XM_011523003.1:c.861G=
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XP_011521305.1:p.Thr287=
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|
XM_011523003.3:c.861G=
|
XP_011521305.1:p.Thr287=
|
|
NM_020988.3:c.987G=
MANE Select
|
NP_066268.1:p.Thr329=
|
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