ENST00000456935.7:c.1519G>T
MANE Select
|
ENSP00000395473.2:p.Ala507Ser
|
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ENST00000221363.8:c.1516G>T
|
ENSP00000221363.4:p.Ala506Ser
|
|
ENST00000433513.5:n.125G>T
|
|
|
ENST00000456935.6:c.1519G>T
|
ENSP00000395473.2:p.Ala507Ser
|
|
ENST00000466794.5:n.1418G>T
|
|
|
ENST00000495617.1:n.695G>T
|
|
|
ENST00000593686.1:c.129G>T
|
|
|
ENST00000595880.5:n.116G>T
|
|
|
NM_000528.3:c.1519G>T
|
NP_000519.2:p.Ala507Ser
|
|
NM_001173498.1:c.1516G>T
|
NP_001166969.1:p.Ala506Ser
|
|
XM_005259913.1:c.1522G>T
|
XP_005259970.1:p.Ala508Ser
|
|
XM_011528017.1:c.418G>T
|
XP_011526319.1:p.Ala140Ser
|
|
XM_005259913.2:c.1522G>T
|
XP_005259970.1:p.Ala508Ser
|
|
XM_024451518.1:c.418G>T
|
XP_024307286.1:p.Ala140Ser
|
|
NM_000528.4:c.1519G>T
MANE Select
|
NP_000519.2:p.Ala507Ser
|
|
NM_001173498.2:c.1516G>T
|
NP_001166969.1:p.Ala506Ser
|
|