NM_002062.5:c.502G>A
MANE Select
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NP_002053.3:p.Gly168Ser
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ENST00000373256.5:c.502G>A
MANE Select
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ENSP00000362353.4:p.Gly168Ser
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NM_002062.3:c.502G>A
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NP_002053.3:p.Gly168Ser
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NM_002062.4:c.502G>A
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NP_002053.3:p.Gly168Ser
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NR_136562.1:n.562G>A
|
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NR_136562.2:n.562G>A
|
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NR_136563.1:n.562G>A
|
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NR_136563.2:n.562G>A
|
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ENST00000373256.4:c.502G>A
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ENSP00000362353.4:p.Gly168Ser
|
XM_017010750.1:c.517G>A
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XP_016866239.1:p.Gly173Ser
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XM_017010751.1:c.517G>A
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XP_016866240.1:p.Gly173Ser
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XR_001743346.1:n.1097G>A
|
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XR_001743347.1:n.1097G>A
|
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XR_001743348.1:n.1097G>A
|
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XR_926153.1:n.562G>A
|
|
XR_926154.1:n.562G>A
|
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XR_926155.1:n.562G>A
|
|