ENST00000578493.2:n.745C>G
|
|
|
ENST00000699291.1:c.537C>G
|
ENSP00000514272.1:p.Gly179=
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|
ENST00000699292.1:n.452C>G
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|
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ENST00000225275.4:c.1412C>G
MANE Select
|
ENSP00000225275.3:p.Ala471Gly
|
|
ENST00000225275.3:c.1412C>G
|
ENSP00000225275.3:p.Ala471Gly
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|
NM_000250.1:c.1412C>G , LRG_84t1:c.1412C>G
|
NP_000241.1:p.Ala471Gly
|
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XM_011524821.1:c.1598C>G
|
XP_011523123.1:p.Ala533Gly
|
|
XM_011524822.1:c.1127C>G
|
XP_011523124.1:p.Ala376Gly
|
|
XM_011524823.1:c.1437C>G
|
XP_011523125.1:p.Gly479=
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|
NM_000250.2:c.1412C>G
MANE Select
|
NP_000241.1:p.Ala471Gly
|
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