ENST00000645828.1:n.2596A>G
|
|
|
ENST00000651671.1:c.4789A>G
MANE Select
|
ENSP00000498587.1:p.Ser1597Gly
|
|
ENST00000679595.1:c.4789A>G
|
ENSP00000506241.1:p.Ser1597Gly
|
|
ENST00000680133.1:c.4675A>G
|
ENSP00000505319.1:p.Ser1559Gly
|
|
ENST00000680218.1:c.4669A>G
|
ENSP00000505339.1:p.Ser1557Gly
|
|
ENST00000680668.1:c.4675A>G
|
ENSP00000506336.1:p.Ser1559Gly
|
|
ENST00000680778.1:c.2386A>G
|
ENSP00000506033.1:p.Ser796Gly
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|
ENST00000680924.1:c.*2189A>G
|
ENSP00000506031.1:n.*2189A>G
|
|
ENST00000681135.1:c.*2398A>G
|
ENSP00000506636.1:n.*2398A>G
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|
ENST00000681298.1:n.1602A>G
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|
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ENST00000681454.1:c.*4025A>G
|
ENSP00000505763.1:n.*4025A>G
|
|
ENST00000277541.6:c.4789A>G
|
ENSP00000277541.6:p.Ser1597Gly
|
|
NM_017617.3:c.4789A>G
|
NP_060087.3:p.Ser1597Gly
|
|
XM_011518717.1:c.4090A>G
|
XP_011517019.1:p.Ser1364Gly
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|
NM_017617.5:c.4789A>G
MANE Select
|
NP_060087.3:p.Ser1597Gly
|
|
XM_011518717.2:c.4066A>G
|
XP_011517019.2:p.Ser1356Gly
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