ENST00000286657.10:c.1698A=
MANE Select
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ENSP00000286657.4:p.Thr566=
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ENST00000286657.8:c.1698A=
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ENSP00000286657.4:p.Thr566=
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|
ENST00000622135.1:c.1698A=
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ENSP00000480055.1:p.Thr566=
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|
NM_014243.2:c.1698A=
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NP_055058.2:p.Thr566=
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|
XM_011532421.1:c.1641A=
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XP_011530723.1:p.Thr547=
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|
XM_011532422.1:c.1614A=
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XP_011530724.1:p.Thr538=
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|
XM_011532423.1:c.1056A=
|
XP_011530725.1:p.Thr352=
|
|
XM_011532424.1:c.966A=
|
XP_011530726.1:p.Thr322=
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|
XM_011532421.2:c.1641A=
|
XP_011530723.1:p.Thr547=
|
|
XM_011532422.3:c.1614A=
|
XP_011530724.1:p.Thr538=
|
|
NM_014243.3:c.1698A=
MANE Select
|
NP_055058.2:p.Thr566=
|
|