ENST00000348911.11:c.4534G=
|
ENSP00000252027.8:p.Gly1512=
|
|
ENST00000418590.4:c.244G=
|
ENSP00000401538.2:p.Gly82=
|
|
ENST00000470434.2:n.1015G=
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|
|
ENST00000684986.1:c.4615G=
|
ENSP00000509117.1:p.Gly1539=
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ENST00000685180.1:n.2488+5449G=
|
|
|
ENST00000685390.1:n.2580G=
|
|
|
ENST00000685411.1:n.362G=
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|
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ENST00000685592.1:c.846G=
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|
|
ENST00000685809.1:c.4525G=
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ENSP00000508863.1:p.Gly1509=
|
|
ENST00000686029.1:c.690G=
|
|
|
ENST00000686191.1:n.3812G=
|
|
|
ENST00000686222.1:c.*4034G=
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ENSP00000508737.1:n.*4034G=
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ENST00000686321.1:c.708G=
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|
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ENST00000686427.1:c.*1547G=
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ENSP00000510379.1:n.*1547G=
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|
ENST00000686758.1:n.2355G=
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|
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ENST00000686801.1:c.4600G=
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ENSP00000509915.1:p.Gly1534=
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ENST00000686826.1:n.931G=
|
|
|
ENST00000687016.1:c.4513G=
|
ENSP00000509074.1:p.Gly1505=
|
|
ENST00000687704.1:c.*2337G=
|
ENSP00000510454.1:n.*2337G=
|
|
ENST00000688066.1:c.4612G=
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ENSP00000510782.1:p.Gly1538=
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|
ENST00000688124.1:c.*3530G=
|
ENSP00000510645.1:n.*3530G=
|
|
ENST00000688848.1:c.*3956G=
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ENSP00000509419.1:n.*3956G=
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|
ENST00000688985.1:c.1613G=
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ENSP00000510477.1:n.1613G=
|
|
ENST00000689129.1:c.4537G=
|
ENSP00000510414.1:p.Gly1513=
|
|
ENST00000689177.1:n.5884G=
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|
|
ENST00000689849.1:c.708G=
|
|
|
ENST00000689981.1:c.4612G=
|
ENSP00000509035.1:p.Gly1538=
|
|
ENST00000690369.1:n.4630G=
|
|
|
ENST00000690590.1:n.1659G=
|
|
|
ENST00000690990.1:c.4606G=
|
ENSP00000510461.1:p.Gly1536=
|
|
ENST00000691233.1:c.4531G=
|
ENSP00000509215.1:p.Gly1511=
|
|
ENST00000691306.1:c.710G=
|
|
|
ENST00000691345.1:n.2302+1131G=
|
|
|
ENST00000691792.1:c.4600G=
|
ENSP00000509911.1:p.Gly1534=
|
|
ENST00000691959.1:n.5331G=
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|
|
ENST00000692844.1:n.1696G=
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|
|
ENST00000692946.1:c.708G=
|
|
|
ENST00000693052.1:c.4630G=
|
ENSP00000509558.1:p.Gly1544=
|
|
ENST00000693289.1:n.1771G=
|
|
|
ENST00000693440.1:c.4609G=
|
ENSP00000509462.1:p.Gly1537=
|
|
ENST00000693499.1:n.5537G=
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|
|
ENST00000693591.1:n.3349G=
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|
|
ENST00000380817.8:c.4612G=
MANE Select
|
ENSP00000370196.2:p.Gly1538=
|
|
ENST00000348911.10:c.4537G=
|
ENSP00000252027.7:p.Gly1513=
|
|
ENST00000380817.7:c.4612G=
|
ENSP00000370196.2:p.Gly1538=
|
|
ENST00000418590.3:c.212G=
|
|
|
ENST00000470434.1:n.753G=
|
|
|
NM_002972.3:c.4612G=
|
NP_002963.2:p.Gly1538=
|
|
XM_005261931.1:c.4615G=
|
XP_005261988.1:p.Gly1539=
|
|
XM_005261935.1:c.4534G=
|
XP_005261992.1:p.Gly1512=
|
|
XM_011530707.1:c.4714G=
|
XP_011529009.1:p.Gly1572=
|
|
XM_011530708.1:c.4666G=
|
XP_011529010.1:p.Gly1556=
|
|
XM_011530709.1:c.4642G=
|
XP_011529011.1:p.Gly1548=
|
|
XM_011530710.1:c.4639G=
|
XP_011529012.1:p.Gly1547=
|
|
XM_011530711.1:c.4639G=
|
XP_011529013.1:p.Gly1547=
|
|
XR_938344.1:n.4732G=
|
|
|
NM_001365819.1:c.4537G=
|
NP_001352748.1:p.Gly1513=
|
|
XM_005261935.2:c.4534G=
|
XP_005261992.1:p.Gly1512=
|
|
XM_011530709.2:c.4642G=
|
XP_011529011.1:p.Gly1548=
|
|
XM_011530710.2:c.4639G=
|
XP_011529012.1:p.Gly1547=
|
|
XM_017028905.2:c.4564G=
|
XP_016884394.1:p.Gly1522=
|
|
NM_002972.4:c.4612G=
MANE Select
|
NP_002963.2:p.Gly1538=
|
|