ENST00000254108.12:c.1565G>A
MANE Select
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ENSP00000254108.8:p.Arg522Lys
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|
ENST00000254108.11:c.1565G>A
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ENSP00000254108.7:p.Arg522Lys
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|
ENST00000380244.7:c.1562G>A
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ENSP00000369594.3:p.Arg521Lys
|
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ENST00000483853.1:n.642G>A
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|
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ENST00000487509.6:n.4740G>A
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|
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ENST00000566605.5:c.*738G>A
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ENSP00000455073.1:n.*738G>A
|
|
ENST00000568685.1:c.1568G>A
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ENSP00000455282.1:p.Arg523Lys
|
|
ENST00000569760.5:n.456G>A
|
|
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NM_001170634.1:c.1562G>A
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NP_001164105.1:p.Arg521Lys
|
|
NM_001170937.1:c.1553G>A
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NP_001164408.1:p.Arg518Lys
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NM_004960.3:c.1565G>A , LRG_655t1:c.1565G>A
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NP_004951.1:p.Arg522Lys
|
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NR_028388.2:n.1635G>A
|
|
|
XM_005255233.3:c.950G>A
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XP_005255290.1:p.Arg317Lys
|
|
XM_011545781.1:c.1559G>A
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XP_011544083.1:p.Arg520Lys
|
|
XM_011545782.1:c.950G>A
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XP_011544084.1:p.Arg317Lys
|
|
XM_005255233.5:c.950G>A
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XP_005255290.1:p.Arg317Lys
|
|
XM_011545782.2:c.950G>A
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XP_011544084.1:p.Arg317Lys
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|
XM_024450221.1:c.1556G>A
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XP_024305989.1:p.Arg519Lys
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|
NM_004960.4:c.1565G>A
MANE Select
|
NP_004951.1:p.Arg522Lys
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