ENST00000254108.12:c.913T>G
MANE Select
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ENSP00000254108.8:p.Phe305Val
|
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ENST00000254108.11:c.913T>G
|
ENSP00000254108.7:p.Phe305Val
|
|
ENST00000380244.7:c.910T>G
|
ENSP00000369594.3:p.Phe304Val
|
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ENST00000474990.5:n.207T>G
|
|
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ENST00000487509.6:n.4088T>G
|
|
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ENST00000564766.1:n.737T>G
|
|
|
ENST00000566605.5:c.*86T>G
|
ENSP00000455073.1:n.*86T>G
|
|
ENST00000568685.1:c.916T>G
|
ENSP00000455282.1:p.Phe306Val
|
|
ENST00000568901.2:n.287T>G
|
|
|
NM_001170634.1:c.910T>G
|
NP_001164105.1:p.Phe304Val
|
|
NM_001170937.1:c.901T>G
|
NP_001164408.1:p.Phe301Val
|
|
NM_004960.3:c.913T>G , LRG_655t1:c.913T>G
|
NP_004951.1:p.Phe305Val
|
|
NR_028388.2:n.983T>G
|
|
|
XM_005255233.3:c.298T>G
|
XP_005255290.1:p.Phe100Val
|
|
XM_011545781.1:c.907T>G
|
XP_011544083.1:p.Phe303Val
|
|
XM_011545782.1:c.298T>G
|
XP_011544084.1:p.Phe100Val
|
|
XM_005255233.5:c.298T>G
|
XP_005255290.1:p.Phe100Val
|
|
XM_011545782.2:c.298T>G
|
XP_011544084.1:p.Phe100Val
|
|
XM_024450221.1:c.904T>G
|
XP_024305989.1:p.Phe302Val
|
|
NM_004960.4:c.913T>G
MANE Select
|
NP_004951.1:p.Phe305Val
|
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