ENST00000254108.12:c.534C>T
MANE Select
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ENSP00000254108.8:p.Gly178=
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ENST00000254108.11:c.534C>T
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ENSP00000254108.7:p.Gly178=
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ENST00000380244.7:c.531C>T
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ENSP00000369594.3:p.Gly177=
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ENST00000487509.6:n.599C>T
|
|
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ENST00000566605.5:c.534C>T
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ENSP00000455073.1:p.Gly178=
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ENST00000568685.1:c.534C>T
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ENSP00000455282.1:p.Gly178=
|
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NM_001170634.1:c.531C>T
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NP_001164105.1:p.Gly177=
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|
NM_001170937.1:c.522C>T
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NP_001164408.1:p.Gly174=
|
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NM_004960.3:c.534C>T , LRG_655t1:c.534C>T
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NP_004951.1:p.Gly178=
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NR_028388.2:n.639C>T
|
|
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XM_005255233.3:c.-47C>T
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XP_005255290.1:n.-47C>T
|
|
XM_011545781.1:c.528C>T
|
XP_011544083.1:p.Gly176=
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|
XM_011545782.1:c.-47C>T
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XP_011544084.1:n.-47C>T
|
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XM_005255233.5:c.-47C>T
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XP_005255290.1:n.-47C>T
|
|
XM_011545782.2:c.-47C>T
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XP_011544084.1:n.-47C>T
|
|
XM_024450221.1:c.525C>T
|
XP_024305989.1:p.Gly175=
|
|
NM_004960.4:c.534C>T
MANE Select
|
NP_004951.1:p.Gly178=
|
|