ENST00000426508.7:c.3308C>G
MANE Select
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ENSP00000406012.2:p.Ala1103Gly
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ENST00000361339.9:c.890C>G
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ENSP00000354895.5:p.Ala297Gly
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ENST00000397417.6:c.*1746C>G
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ENSP00000380562.2:n.*1746C>G
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ENST00000426508.6:c.3308C>G
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ENSP00000406012.2:p.Ala1103Gly
|
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ENST00000565298.5:n.3132C>G
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NM_014714.3:c.3308C>G
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NP_055529.2:p.Ala1103Gly
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XM_006720989.2:c.3308C>G
|
XP_006721052.1:p.Ala1103Gly
|
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XM_006720990.2:c.3308C>G
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XP_006721053.1:p.Ala1103Gly
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XM_006720991.2:c.3308C>G
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XP_006721054.1:p.Ala1103Gly
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XM_006720992.2:c.941C>G
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XP_006721055.1:p.Ala314Gly
|
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XM_011522766.1:c.3062C>G
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XP_011521068.1:p.Ala1021Gly
|
|
XM_011522767.1:c.2333C>G
|
XP_011521069.1:p.Ala778Gly
|
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XM_006720990.3:c.3308C>G
|
XP_006721053.1:p.Ala1103Gly
|
|
XM_006720991.3:c.3308C>G
|
XP_006721054.1:p.Ala1103Gly
|
|
XM_006720992.3:c.941C>G
|
XP_006721055.1:p.Ala314Gly
|
|
XM_011522766.3:c.3062C>G
|
XP_011521068.1:p.Ala1021Gly
|
|
XM_011522767.2:c.2333C>G
|
XP_011521069.1:p.Ala778Gly
|
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XM_017023910.1:c.3308C>G
|
XP_016879399.1:p.Ala1103Gly
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XM_017023911.1:c.1493C>G
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XP_016879400.1:p.Ala498Gly
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NM_014714.4:c.3308C>G
MANE Select
|
NP_055529.2:p.Ala1103Gly
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