ENST00000356231.4:c.1804G>T
MANE Select
|
ENSP00000348564.3:p.Ala602Ser
|
|
ENST00000643434.1:c.*982G>T
|
ENSP00000494699.1:n.*982G>T
|
|
ENST00000356231.3:c.1804G>T
|
ENSP00000348564.3:p.Ala602Ser
|
|
NM_138477.2:c.1804G>T
|
NP_612486.2:p.Ala602Ser
|
|
XM_005254176.3:c.1807G>T
|
XP_005254233.1:p.Ala603Ser
|
|
XM_011521270.1:c.1831G>T
|
XP_011519572.1:p.Ala611Ser
|
|
XM_011521271.1:c.1828G>T
|
XP_011519573.1:p.Ala610Ser
|
|
XM_011521272.1:c.1831G>T
|
XP_011519574.1:p.Ala611Ser
|
|
XM_011521273.1:c.1831G>T
|
XP_011519575.1:p.Ala611Ser
|
|
XM_011521274.1:c.796G>T
|
XP_011519576.1:p.Ala266Ser
|
|
XM_011521275.1:c.1048G>T
|
XP_011519577.1:p.Ala350Ser
|
|
XR_931757.1:n.1842G>T
|
|
|
NM_138477.4:c.1804G>T
MANE Select
|
NP_612486.2:p.Ala602Ser
|
|
XM_005254176.5:c.1807G>T
|
XP_005254233.1:p.Ala603Ser
|
|
XM_011521270.2:c.1831G>T
|
XP_011519572.1:p.Ala611Ser
|
|
XM_011521271.2:c.1828G>T
|
XP_011519573.1:p.Ala610Ser
|
|
XM_011521274.2:c.796G>T
|
XP_011519576.1:p.Ala266Ser
|
|
XR_001751104.1:n.1861G>T
|
|
|
XR_001751105.1:n.1861G>T
|
|
|
XR_931757.2:n.1862G>T
|
|
|