ENST00000645828.1:n.2569A>G
|
|
|
ENST00000651671.1:c.4762A>G
MANE Select
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ENSP00000498587.1:p.Ser1588Gly
|
|
ENST00000679595.1:c.4762A>G
|
ENSP00000506241.1:p.Ser1588Gly
|
|
ENST00000680133.1:c.4648A>G
|
ENSP00000505319.1:p.Ser1550Gly
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|
ENST00000680218.1:c.4642A>G
|
ENSP00000505339.1:p.Ser1548Gly
|
|
ENST00000680668.1:c.4648A>G
|
ENSP00000506336.1:p.Ser1550Gly
|
|
ENST00000680778.1:c.2359A>G
|
ENSP00000506033.1:p.Ser787Gly
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|
ENST00000680924.1:c.*2162A>G
|
ENSP00000506031.1:n.*2162A>G
|
|
ENST00000681135.1:c.*2371A>G
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ENSP00000506636.1:n.*2371A>G
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ENST00000681298.1:n.1575A>G
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|
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ENST00000681454.1:c.*3998A>G
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ENSP00000505763.1:n.*3998A>G
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|
ENST00000277541.6:c.4762A>G
|
ENSP00000277541.6:p.Ser1588Gly
|
|
NM_017617.3:c.4762A>G
|
NP_060087.3:p.Ser1588Gly
|
|
XM_011518717.1:c.4063A>G
|
XP_011517019.1:p.Ser1355Gly
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|
NM_017617.5:c.4762A>G
MANE Select
|
NP_060087.3:p.Ser1588Gly
|
|
XM_011518717.2:c.4039A>G
|
XP_011517019.2:p.Ser1347Gly
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