ENST00000449082.3:c.4906G=
MANE Select
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ENSP00000390600.2:p.Ala1636=
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ENST00000643924.1:c.4903G=
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ENSP00000495595.1:p.Ala1635=
|
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ENST00000655275.1:c.4930G=
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ENSP00000499510.1:p.Ala1644=
|
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ENST00000449082.2:c.4906G=
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ENSP00000390600.2:p.Ala1636=
|
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NM_001293306.2:c.4903G=
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NP_001280235.2:p.Ala1635=
|
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NM_001293307.2:c.4612G=
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NP_001280236.2:p.Ala1538=
|
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NM_006514.3:c.4906G=
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NP_006505.3:p.Ala1636=
|
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XM_005265371.2:c.4915G=
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XP_005265428.1:p.Ala1639=
|
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XM_011533993.1:c.4912G=
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XP_011532295.1:p.Ala1638=
|
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XM_011533994.1:c.4621G=
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XP_011532296.1:p.Ala1541=
|
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XM_005265371.3:c.4915G=
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XP_005265428.1:p.Ala1639=
|
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XM_011533993.2:c.4912G=
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XP_011532295.1:p.Ala1638=
|
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XM_011533994.2:c.4621G=
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XP_011532296.1:p.Ala1541=
|
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NM_006514.4:c.4906G=
MANE Select
|
NP_006505.4:p.Ala1636=
|
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