ENST00000456935.7:c.2695T>G
MANE Select
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ENSP00000395473.2:p.Ser899Ala
|
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ENST00000221363.8:c.2692T>G
|
ENSP00000221363.4:p.Ser898Ala
|
|
ENST00000456935.6:c.2695T>G
|
ENSP00000395473.2:p.Ser899Ala
|
|
ENST00000466794.5:n.3285T>G
|
|
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ENST00000469423.1:n.17T>G
|
|
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ENST00000493218.5:n.106T>G
|
|
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ENST00000597692.1:c.254T>G
|
|
|
NM_000528.3:c.2695T>G
|
NP_000519.2:p.Ser899Ala
|
|
NM_001173498.1:c.2692T>G
|
NP_001166969.1:p.Ser898Ala
|
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XM_005259913.1:c.2698T>G
|
XP_005259970.1:p.Ser900Ala
|
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XM_011528017.1:c.1594T>G
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XP_011526319.1:p.Ser532Ala
|
|
XM_005259913.2:c.2698T>G
|
XP_005259970.1:p.Ser900Ala
|
|
XM_024451518.1:c.1594T>G
|
XP_024307286.1:p.Ser532Ala
|
|
NM_000528.4:c.2695T>G
MANE Select
|
NP_000519.2:p.Ser899Ala
|
|
NM_001173498.2:c.2692T>G
|
NP_001166969.1:p.Ser898Ala
|
|