ENST00000529510.6:n.1018G=
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|
|
ENST00000697845.1:n.1798G=
|
|
|
ENST00000697846.1:n.1018G=
|
|
|
ENST00000697847.1:n.1202-320G=
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|
|
ENST00000697848.1:n.1104G=
|
|
|
ENST00000697849.1:n.2913G=
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|
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ENST00000697850.1:n.1104G=
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|
|
ENST00000697851.1:n.2712G=
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|
|
ENST00000638186.1:n.1178G=
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|
ENST00000638360.1:n.1010G=
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|
|
ENST00000638925.1:n.1143G=
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|
|
ENST00000650539.1:n.1280G=
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|
|
ENST00000330775.9:c.874G=
|
ENSP00000476242.2:p.Gly292=
|
|
ENST00000357590.9:c.874G=
|
ENSP00000476176.2:p.Gly292=
|
|
ENST00000524428.5:n.1110G=
|
|
|
ENST00000525039.5:n.1298G=
|
|
|
ENST00000525102.5:n.1632G=
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|
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ENST00000525372.5:n.972G=
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|
|
ENST00000526275.5:n.1656G=
|
|
|
ENST00000527992.5:n.1102G=
|
|
|
ENST00000529510.5:n.562G=
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|
|
ENST00000530407.5:n.1024G=
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|
|
ENST00000532085.1:n.4255G=
|
|
|
ENST00000538950.5:c.655G=
|
ENSP00000475991.2:p.Gly219=
|
|
ENST00000545985.5:c.874G=
|
ENSP00000475241.2:p.Gly292=
|
|
NM_001164277.1:c.874G= , LRG_187t1:c.874G=
|
NP_001157749.1:p.Gly292=
|
|
NM_001164278.1:c.874G=
|
NP_001157750.1:p.Gly292=
|
|
NM_001164279.1:c.655G=
|
NP_001157751.1:p.Gly219=
|
|
NM_001164280.1:c.874G=
|
NP_001157752.1:p.Gly292=
|
|
NM_001467.5:c.874G=
|
NP_001458.1:p.Gly292=
|
|
NM_001164278.2:c.874G=
|
NP_001157750.1:p.Gly292=
|
|
NM_001164279.2:c.655G=
|
NP_001157751.1:p.Gly219=
|
|
NM_001164280.2:c.874G=
|
NP_001157752.1:p.Gly292=
|
|
NM_001467.6:c.874G=
|
NP_001458.1:p.Gly292=
|
|
NM_001164277.2:c.874G=
MANE Select
|
NP_001157749.1:p.Gly292=
|
|