ENST00000262367.10:c.6181A>G
MANE Select
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ENSP00000262367.5:p.Ser2061Gly
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ENST00000262367.9:c.6181A>G
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ENSP00000262367.5:p.Ser2061Gly
|
|
ENST00000382070.7:c.6067A>G
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ENSP00000371502.3:p.Ser2023Gly
|
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NM_001079846.1:c.6067A>G
|
NP_001073315.1:p.Ser2023Gly
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|
NM_004380.2:c.6181A>G
|
NP_004371.2:p.Ser2061Gly
|
|
XM_005255124.3:c.6136A>G
|
XP_005255181.1:p.Ser2046Gly
|
|
XM_005255125.3:c.5764A>G
|
XP_005255182.1:p.Ser1922Gly
|
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XM_006720848.2:c.5920A>G
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XP_006720911.1:p.Ser1974Gly
|
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XM_011522380.1:c.6127A>G
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XP_011520682.1:p.Ser2043Gly
|
|
XM_011522381.1:c.5428A>G
|
XP_011520683.1:p.Ser1810Gly
|
|
XM_005255124.4:c.6136A>G
|
XP_005255181.1:p.Ser2046Gly
|
|
XM_005255125.4:c.5764A>G
|
XP_005255182.1:p.Ser1922Gly
|
|
XM_006720848.3:c.5920A>G
|
XP_006720911.1:p.Ser1974Gly
|
|
XM_011522381.2:c.5428A>G
|
XP_011520683.1:p.Ser1810Gly
|
|
XM_017022944.1:c.6175A>G
|
XP_016878433.1:p.Ser2059Gly
|
|
NM_004380.3:c.6181A>G
MANE Select
|
NP_004371.2:p.Ser2061Gly
|
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