ENST00000328194.8:c.3621T>C
MANE Select
|
ENSP00000328524.3:p.Asn1207=
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ENST00000525784.6:n.1483T>C
|
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ENST00000530780.2:c.*3447T>C
|
ENSP00000433925.1:n.*3447T>C
|
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ENST00000531747.2:n.3292T>C
|
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ENST00000679446.1:n.3542T>C
|
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ENST00000679458.1:n.5022T>C
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ENST00000679460.1:n.4683T>C
|
|
|
ENST00000679568.1:c.3621T>C
|
ENSP00000505860.1:p.Asn1207=
|
|
ENST00000679745.1:n.4126T>C
|
|
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ENST00000679773.1:n.2782T>C
|
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ENST00000679926.1:n.4923T>C
|
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ENST00000679999.1:c.*678T>C
|
ENSP00000505198.1:n.*678T>C
|
|
ENST00000680252.1:c.3288T>C
|
|
|
ENST00000680294.1:c.3414T>C
|
ENSP00000506113.1:p.Asn1138=
|
|
ENST00000680358.1:n.2920T>C
|
|
|
ENST00000680470.1:c.*1402T>C
|
ENSP00000505975.1:n.*1402T>C
|
|
ENST00000680554.1:c.*154T>C
|
ENSP00000505621.1:n.*154T>C
|
|
ENST00000680576.1:n.5097T>C
|
|
|
ENST00000680599.1:n.3662T>C
|
|
|
ENST00000680742.1:c.*154T>C
|
ENSP00000505206.1:n.*154T>C
|
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ENST00000680791.1:n.2505T>C
|
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ENST00000680885.1:n.5323T>C
|
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ENST00000681158.1:c.3205T>C
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|
|
ENST00000681203.1:c.3549T>C
|
ENSP00000506456.1:p.Asn1183=
|
|
ENST00000681371.1:n.3493T>C
|
|
|
ENST00000681425.1:n.4099T>C
|
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ENST00000681639.1:n.1900T>C
|
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|
ENST00000328194.7:c.3621T>C
|
ENSP00000328524.3:p.Asn1207=
|
|
ENST00000525784.5:c.557T>C
|
|
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ENST00000527700.5:n.3183T>C
|
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ENST00000528725.5:c.317T>C
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ENST00000529977.5:n.1522T>C
|
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|
ENST00000530044.5:c.3621T>C
|
ENSP00000435866.1:p.Asn1207=
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ENST00000531747.1:c.857T>C
|
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ENST00000533737.5:c.284T>C
|
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|
NM_001243254.1:c.3621T>C
|
NP_001230183.1:p.Asn1207=
|
|
NM_015213.3:c.3621T>C
|
NP_056028.2:p.Asn1207=
|
|
XM_005252832.1:c.3621T>C
|
XP_005252889.1:p.Asn1207=
|
|
XM_011519952.1:c.3621T>C
|
XP_011518254.1:p.Asn1207=
|
|
XM_011519953.1:c.1719T>C
|
XP_011518255.1:p.Asn573=
|
|
XR_242782.2:n.3803T>C
|
|
|
XR_930851.1:n.3803T>C
|
|
|
NM_001348749.1:c.3549T>C
|
NP_001335678.1:p.Asn1183=
|
|
NM_001348750.1:c.3333T>C
|
NP_001335679.1:p.Asn1111=
|
|
NR_145966.2:n.3795T>C
|
|
|
NM_015213.4:c.3621T>C
MANE Select
|
NP_056028.2:p.Asn1207=
|
|
NM_001243254.2:c.3621T>C
|
NP_001230183.1:p.Asn1207=
|
|
NM_001348749.2:c.3549T>C
|
NP_001335678.1:p.Asn1183=
|
|
NM_001348750.2:c.3333T>C
|
NP_001335679.1:p.Asn1111=
|
|