ENST00000241453.12:c.2039C>G
MANE Select
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ENSP00000241453.7:p.Ala680Gly
|
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ENST00000241453.11:c.2039C>G
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ENSP00000241453.7:p.Ala680Gly
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ENST00000380987.2:c.2039C>G
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ENSP00000370374.2:p.Ala680Gly
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NM_004119.2:c.2039C>G , LRG_457t1:c.2039C>G
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NP_004110.2:p.Ala680Gly
|
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NR_130706.1:n.2121C>G
|
|
|
XM_011535015.1:c.1982C>G
|
XP_011533317.1:p.Ala661Gly
|
|
XM_011535016.1:c.1514C>G
|
XP_011533318.1:p.Ala505Gly
|
|
XM_011535017.1:c.1514C>G
|
XP_011533319.1:p.Ala505Gly
|
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XM_011535018.1:c.1514C>G
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XP_011533320.1:p.Ala505Gly
|
|
XM_011535015.2:c.1982C>G
|
XP_011533317.1:p.Ala661Gly
|
|
XM_011535017.2:c.1514C>G
|
XP_011533319.1:p.Ala505Gly
|
|
XM_011535018.2:c.1514C>G
|
XP_011533320.1:p.Ala505Gly
|
|
XM_017020486.1:c.1823C>G
|
XP_016875975.1:p.Ala608Gly
|
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XM_017020487.1:c.1514C>G
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XP_016875976.1:p.Ala505Gly
|
|
XM_017020488.1:c.1160C>G
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XP_016875977.1:p.Ala387Gly
|
|
XM_017020489.1:c.1142C>G
|
XP_016875978.1:p.Ala381Gly
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NM_004119.3:c.2039C>G
MANE Select
|
NP_004110.2:p.Ala680Gly
|
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NR_130706.2:n.2105C>G
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|
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