ENST00000504915.3:c.5065G=
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ENSP00000473355.2:p.Ala1689=
|
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ENST00000505350.2:c.*5017G=
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ENSP00000481752.1:n.*5017G=
|
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ENST00000507379.6:c.4957G=
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ENSP00000423224.2:p.Ala1653=
|
|
ENST00000509732.6:c.5011G=
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ENSP00000426541.2:p.Ala1671=
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ENST00000512211.7:c.5011G=
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ENSP00000423828.3:p.Ala1671=
|
|
ENST00000257430.9:c.5011G=
MANE Select
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ENSP00000257430.4:p.Ala1671=
|
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ENST00000257430.8:c.5011G=
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ENSP00000257430.4:p.Ala1671=
|
|
ENST00000508376.6:c.5011G=
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ENSP00000427089.2:p.Ala1671=
|
|
ENST00000508624.5:c.*4333G=
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ENSP00000424265.1:n.*4333G=
|
|
ENST00000520401.1:c.230+11633G=
|
|
|
NM_000038.5:c.5011G=
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NP_000029.2:p.Ala1671=
|
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NM_001127510.2:c.5011G=
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NP_001120982.1:p.Ala1671=
|
|
NM_001127511.2:c.4957G=
|
NP_001120983.2:p.Ala1653=
|
|
NM_001354895.1:c.5011G=
|
NP_001341824.1:p.Ala1671=
|
|
NM_001354896.1:c.5065G=
|
NP_001341825.1:p.Ala1689=
|
|
NM_001354897.1:c.5041G=
|
NP_001341826.1:p.Ala1681=
|
|
NM_001354898.1:c.4936G=
|
NP_001341827.1:p.Ala1646=
|
|
NM_001354899.1:c.4927G=
|
NP_001341828.1:p.Ala1643=
|
|
NM_001354900.1:c.4888G=
|
NP_001341829.1:p.Ala1630=
|
|
NM_001354901.1:c.4834G=
|
NP_001341830.1:p.Ala1612=
|
|
NM_001354902.1:c.4738G=
|
NP_001341831.1:p.Ala1580=
|
|
NM_001354903.1:c.4708G=
|
NP_001341832.1:p.Ala1570=
|
|
NM_001354904.1:c.4633G=
|
NP_001341833.1:p.Ala1545=
|
|
NM_001354905.1:c.4531G=
|
NP_001341834.1:p.Ala1511=
|
|
NM_001354906.1:c.4162G=
|
NP_001341835.1:p.Ala1388=
|
|
NM_000038.6:c.5011G=
MANE Select
|
NP_000029.2:p.Ala1671=
|
|
NM_001127510.3:c.5011G=
|
NP_001120982.1:p.Ala1671=
|
|
NM_001127511.3:c.4957G=
|
NP_001120983.2:p.Ala1653=
|
|
NM_001354895.2:c.5011G=
|
NP_001341824.1:p.Ala1671=
|
|
NM_001354896.2:c.5065G=
|
NP_001341825.1:p.Ala1689=
|
|
NM_001354897.2:c.5041G=
|
NP_001341826.1:p.Ala1681=
|
|
NM_001354898.2:c.4936G=
|
NP_001341827.1:p.Ala1646=
|
|
NM_001354899.2:c.4927G=
|
NP_001341828.1:p.Ala1643=
|
|
NM_001354900.2:c.4888G=
|
NP_001341829.1:p.Ala1630=
|
|
NM_001354901.2:c.4834G=
|
NP_001341830.1:p.Ala1612=
|
|
NM_001354902.2:c.4738G=
|
NP_001341831.1:p.Ala1580=
|
|
NM_001354903.2:c.4708G=
|
NP_001341832.1:p.Ala1570=
|
|
NM_001354904.2:c.4633G=
|
NP_001341833.1:p.Ala1545=
|
|
NM_001354905.2:c.4531G=
|
NP_001341834.1:p.Ala1511=
|
|
NM_001354906.2:c.4162G=
|
NP_001341835.1:p.Ala1388=
|
|