ENST00000529510.6:n.1014+313G>A
|
|
|
ENST00000697845.1:n.1251G>A
|
|
|
ENST00000697846.1:n.1014+313G>A
|
|
|
ENST00000697847.1:n.1079G>A
|
|
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ENST00000697848.1:n.1079G>A
|
|
|
ENST00000697849.1:n.2366G>A
|
|
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ENST00000697850.1:n.1079G>A
|
|
|
ENST00000697851.1:n.2687G>A
|
|
|
ENST00000638186.1:n.1153G>A
|
|
|
ENST00000638360.1:n.985G>A
|
|
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ENST00000638925.1:n.1086G>A
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|
|
ENST00000650539.1:n.1255G>A
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|
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ENST00000330775.9:c.849G>A
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ENSP00000476242.2:p.Leu283=
|
|
ENST00000357590.9:c.849G>A
|
ENSP00000476176.2:p.Leu283=
|
|
ENST00000524428.5:n.1106+313G>A
|
|
|
ENST00000525039.5:n.1273G>A
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|
|
ENST00000525102.5:n.1607G>A
|
|
|
ENST00000525372.5:n.850G>A
|
|
|
ENST00000526275.5:n.1631G>A
|
|
|
ENST00000527992.5:n.1077G>A
|
|
|
ENST00000529510.5:n.558+313G>A
|
|
|
ENST00000530407.5:n.999G>A
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|
|
ENST00000532085.1:n.3708G>A
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|
|
ENST00000538950.5:c.630G>A
|
ENSP00000475991.2:p.Leu210=
|
|
ENST00000545985.5:c.849G>A
|
ENSP00000475241.2:p.Leu283=
|
|
NM_001164277.1:c.849G>A , LRG_187t1:c.849G>A
|
NP_001157749.1:p.Leu283=
|
|
NM_001164278.1:c.849G>A
|
NP_001157750.1:p.Leu283=
|
|
NM_001164279.1:c.630G>A
|
NP_001157751.1:p.Leu210=
|
|
NM_001164280.1:c.849G>A
|
NP_001157752.1:p.Leu283=
|
|
NM_001467.5:c.849G>A
|
NP_001458.1:p.Leu283=
|
|
NM_001164278.2:c.849G>A
|
NP_001157750.1:p.Leu283=
|
|
NM_001164279.2:c.630G>A
|
NP_001157751.1:p.Leu210=
|
|
NM_001164280.2:c.849G>A
|
NP_001157752.1:p.Leu283=
|
|
NM_001467.6:c.849G>A
|
NP_001458.1:p.Leu283=
|
|
NM_001164277.2:c.849G>A
MANE Select
|
NP_001157749.1:p.Leu283=
|
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