ENST00000261647.10:c.152G=
MANE Select
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ENSP00000261647.5:p.Gly51=
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ENST00000261647.9:c.152G=
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ENSP00000261647.5:p.Gly51=
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|
ENST00000466729.5:c.217G=
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|
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ENST00000470399.1:c.167G=
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ENSP00000465082.1:p.Gly56=
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ENST00000475723.5:c.199G=
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|
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ENST00000497842.6:n.177G=
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|
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ENST00000583704.1:n.177G=
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|
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NM_001271420.1:c.-307G=
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NP_001258349.1:n.-307G=
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|
NM_017775.3:c.152G=
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NP_060245.3:p.Gly51=
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XM_011523950.1:c.152G=
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XP_011522252.1:p.Gly51=
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XM_017024801.2:c.152G=
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XP_016880290.2:p.Gly51=
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|
XM_017024802.2:c.152G=
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XP_016880291.2:p.Gly51=
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|
XM_024450814.1:c.152G=
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XP_024306582.1:p.Gly51=
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|
NM_017775.4:c.152G=
MANE Select
|
NP_060245.3:p.Gly51=
|
|
NM_001271420.2:c.-307G=
|
NP_001258349.1:n.-307G=
|
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