ENST00000281928.9:c.4376T>G
MANE Select
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ENSP00000281928.3:p.Val1459Gly
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ENST00000549786.2:c.3804T>G
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ENST00000648379.1:n.2744T>G
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ENST00000648737.1:n.4140T>G
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ENST00000648825.1:n.1116T>G
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ENST00000648916.1:n.2387T>G
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ENST00000649146.1:n.1106T>G
|
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ENST00000649607.1:c.2560T>G
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ENST00000649775.1:c.873T>G
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ENST00000650091.1:n.2352T>G
|
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ENST00000650226.1:c.4376T>G
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ENSP00000496981.1:p.Val1459Gly
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ENST00000281928.7:c.4376T>G
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ENSP00000281928.3:p.Val1459Gly
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NM_015335.4:c.4376T>G
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NP_056150.1:p.Val1459Gly
|
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XM_011538080.1:c.4376T>G
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XP_011536382.1:p.Val1459Gly
|
|
XM_011538081.1:c.4373T>G
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XP_011536383.1:p.Val1458Gly
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XM_011538082.1:c.4346T>G
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XP_011536384.1:p.Val1449Gly
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XM_011538080.2:c.4376T>G
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XP_011536382.1:p.Val1459Gly
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XM_011538081.2:c.4373T>G
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XP_011536383.1:p.Val1458Gly
|
|
XM_011538082.2:c.4346T>G
|
XP_011536384.1:p.Val1449Gly
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XM_017019090.1:c.4373T>G
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XP_016874579.1:p.Val1458Gly
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NM_015335.5:c.4376T>G
MANE Select
|
NP_056150.1:p.Val1459Gly
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